Publications
Ancient founder mutation in RUBCN: a second unrelated family confirms Salih ataxia (SCAR15)
Case study of SCAR-15 in Saudi Arabian family
Published: May 25, 2020
Authors: Mohammed Z. Seidahmed, Muddathir H. Hamad, Albandary AlBakheet, Salah A. Elmalik, Abdulmajeed AlDrees, Jumanah Al-Sufayan, Ibrahim Alorainy, Ibrahim M. Ghozzi, Dilek Colak, Mustafa A. Salih, Namik Kaya
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15
Entry of SCAR-15 into database of genetic disorders.
Published: March 24, 2014, Last updated: September 11, 2020
Authors: Original publisher: Cassandra L. Kniffin, Last edit by: Hilary J. Vernon
Autosomal Recessive Spinocerebellar Ataxia 15
Entry of SCAR-15 into National Organization for Rare Disorders
The Salih Ataxia Mutation Impairs Rubicon Endosomal Localization
Research article about the causes of Salih Ataxia, another term for SCAR-15
Published: June 1, 2013
Authors: M. Assoum, M. A. Salih, N. Drouot, K. Hnia, A. Martelli, M. Koenig