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Founder mutation in RUBCN gene in a second family confirms Salih ataxia (scar15)
Journal article   Peer reviewed

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

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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