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

Salih, Mustafa A.; Hamad, Muddathir H.; Seidahmed, Mohammed Zain; Binbakheet, A.; Alorainy, Ibrahim A.; Kaya, Namik

doi:10.1016/j.jns.2019.10.1558

Journal of the Neurological Sciences

2019

DOI: 10.1016/j.jns.2019.10.1558

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

Mustafa A. Salih

Muddathir H. Hamad

Mohammed Zain Seidahmed

et al.

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

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