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Case series of autosomal recessive hereditary spastic paraparesis with novel mutation in SPG 7 gene
Shakya Bhattacharjee, Nicholas Beauchamp, Brian E. Murray and Timothy Lynch
Neurosciences Journal October 2017, 22 (4) 303-307; DOI: https://doi.org/10.17712/nsj.2017.4.20170253
Shakya Bhattacharjee
From the Department of Neurology (Bhattacharjee), from Plymouth Hospital NHS Trust, Department of Neurology (Bhattacharjee), Plymouth Hospital NHS Trust, from Sheffield Diagnostic Genetics Service (Beauchamp), Sheffield Children’s NHS Foundation Trust, Sheffield, United Kingdom, and from Hermitage Medical Clinic (Murray), Mater University Hospital and Dublin Neurological Institute (Lynch), Dublin, Ireland
MBBS, MRCPNicholas Beauchamp
From the Department of Neurology (Bhattacharjee), from Plymouth Hospital NHS Trust, Department of Neurology (Bhattacharjee), Plymouth Hospital NHS Trust, from Sheffield Diagnostic Genetics Service (Beauchamp), Sheffield Children’s NHS Foundation Trust, Sheffield, United Kingdom, and from Hermitage Medical Clinic (Murray), Mater University Hospital and Dublin Neurological Institute (Lynch), Dublin, Ireland
PhDBrian E. Murray
From the Department of Neurology (Bhattacharjee), from Plymouth Hospital NHS Trust, Department of Neurology (Bhattacharjee), Plymouth Hospital NHS Trust, from Sheffield Diagnostic Genetics Service (Beauchamp), Sheffield Children’s NHS Foundation Trust, Sheffield, United Kingdom, and from Hermitage Medical Clinic (Murray), Mater University Hospital and Dublin Neurological Institute (Lynch), Dublin, Ireland
ABPN, AANEMTimothy Lynch
From the Department of Neurology (Bhattacharjee), from Plymouth Hospital NHS Trust, Department of Neurology (Bhattacharjee), Plymouth Hospital NHS Trust, from Sheffield Diagnostic Genetics Service (Beauchamp), Sheffield Children’s NHS Foundation Trust, Sheffield, United Kingdom, and from Hermitage Medical Clinic (Murray), Mater University Hospital and Dublin Neurological Institute (Lynch), Dublin, Ireland
FRCP, ABPN![Loading Loading](https://nsj.org.sa/sites/all/modules/contrib/panels_ajax_tab/images/loading.gif)
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In this issue
Case series of autosomal recessive hereditary spastic paraparesis with novel mutation in SPG 7 gene
Shakya Bhattacharjee, Nicholas Beauchamp, Brian E. Murray, Timothy Lynch
Neurosciences Journal Oct 2017, 22 (4) 303-307; DOI: 10.17712/nsj.2017.4.20170253
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