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Brief ReportBrief Communication
Open Access

Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family

Muhammad I. Naseer, Mahmood Rasool, Angham A. Abdulkareem, Randa I. Bassiouni, Hussein Algahtani, Adeel G. Chaudhary and Mohammad H. Al-Qahtani
Neurosciences Journal October 2018, 23 (4) 346-350; DOI: https://doi.org/10.17712/nsj.2018.4.20180095
Muhammad I. Naseer
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
M.phil, PhD
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Mahmood Rasool
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
PhD
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Angham A. Abdulkareem
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
PhD student
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Randa I. Bassiouni
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
MD
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Hussein Algahtani
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
MD, FRCPS
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Adeel G. Chaudhary
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
PhD
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Mohammad H. Al-Qahtani
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
PhD
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  • For correspondence: [email protected]
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Article Information

vol. 23 no. 4 346-350
DOI 
https://doi.org/10.17712/nsj.2018.4.20180095
PubMed 
30351297

Published By 
Neurosciences Journal
Online ISSN 
1658-3183
History 
  • Received February 25, 2018
  • Accepted September 12, 2018
  • Published online November 13, 2020.

Copyright & Usage 
Copyright: © Neurosciences Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work.

Author Information

  1. Muhammad I. Naseer, M.phil, PhD,
  2. Mahmood Rasool, PhD,
  3. Angham A. Abdulkareem, PhD student,
  4. Randa I. Bassiouni, MD,
  5. Hussein Algahtani, MD, FRCPS,
  6. Adeel G. Chaudhary, PhD and
  7. Mohammad H. Al-Qahtani, PhD⇑
  1. From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
  1. Address correspondence and reprint requests to: Dr. Muhammad I. Naseer, Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia. E-mail: mimrannaseer{at}yahoo.com ORCID ID: orcid.org/0000-0002-9343-5825
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Neurosciences Journal: 23 (4)
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Vol. 23, Issue 4
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Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family
Muhammad I. Naseer, Mahmood Rasool, Angham A. Abdulkareem, Randa I. Bassiouni, Hussein Algahtani, Adeel G. Chaudhary, Mohammad H. Al-Qahtani
Neurosciences Journal Oct 2018, 23 (4) 346-350; DOI: 10.17712/nsj.2018.4.20180095

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Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family
Muhammad I. Naseer, Mahmood Rasool, Angham A. Abdulkareem, Randa I. Bassiouni, Hussein Algahtani, Adeel G. Chaudhary, Mohammad H. Al-Qahtani
Neurosciences Journal Oct 2018, 23 (4) 346-350; DOI: 10.17712/nsj.2018.4.20180095
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© 2025 Neurosciences Journal Neurosciences is copyright under the Berne Convention and the International Copyright Convention. All rights reserved. Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3183. Print ISSN 1319-6138.

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