Founder mutation in RUBCN gene in a second family confirms Salih ataxia (scar15)

Journal article

Peer reviewed

M. Salih, M. Hamad, M. Seidahmed, A. Binbakheet, I. Alorainy and N. Kaya

Journal of the neurological sciences, Vol.405, pp.7-7

15/10/2019

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Title: Founder mutation in RUBCN gene in a second family confirms Salih ataxia (scar15)
Creators - without role: M. Salih - King Saud University
M. Hamad - King Saud University
M. Seidahmed - Security Forces Hospital
A. Binbakheet - King Faisal Specialist Hospital & Research Centre
I. Alorainy - King Saud University
N. Kaya - King Faisal Specialist Hospital & Research Centre
Publication Details: Journal of the neurological sciences, Vol.405, pp.7-7
Publisher: Elsevier B.V
Identifiers: 9924238708331
Academic Unit: King Saud University
Language: English
Resource Type: Journal article