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

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Bibliographic Details
Published in:Journal of the neurological sciences 2019-10, Vol.405, p.7-7
Main Authors: Salih, M., Hamad, M., Seidahmed, M., Binbakheet, A., Alorainy, I., Kaya, N.
Format: Article
Language:English
Online Access:Get full text
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ISSN:0022-510X
1878-5883
DOI:10.1016/j.jns.2019.10.1558