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  A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature
 
 
Title: A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature
Author: Al-Muhaizea, Mohammad A.
AlMutairi, Faten
Almass, Rawan
AlHarthi, Safinaz
Aldosary, Mazhor S.
Alsagob, Maysoon
AlOdaib, Ali
Colak, Dilek
Kaya, Namik
Appeared in: The cerebellum
Paging: Volume 17 (2017) nr. 3 pages 276-285
Year: 2017
Contents:
Publisher: Springer US, New York
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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