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Page 1
Clinical and genetic features of anoctaminopathy in Saudi Arabia.
Neurosciences (Riyadh). 2015 Apr;20(2):173-7. doi: 10.17712/nsj.2015.2.20140547.
Neurosciences (Riyadh). 2015.
PMID: 25864073
Free PMC article.
LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation.
Bohlega SA, Alfawaz S, Abou-Al-Shaar H, Al-Hindi HN, Murad HN, Bohlega MS, Meyer BF, Monies D.
Bohlega SA, et al. Among authors: murad hn.
Acta Myol. 2018 Sep 1;37(3):221-226. eCollection 2018 Sep.
Acta Myol. 2018.
PMID: 30838352
Free PMC article.
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Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis.
Wakil SM, Murad HN, Baz BM, Hagos ST, Al-Amr RA, Al-Yamani SA, Al-Wadaee SM, Meyer BF, Bohlega SA.
Wakil SM, et al. Among authors: murad hn.
Neurosciences (Riyadh). 2012 Jan;17(1):48-52.
Neurosciences (Riyadh). 2012.
PMID: 22246010
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