Movement disorders in spinocerebellar ataxias
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.23584/fullpdf
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4. A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter;Yamashita;Ann Neurol,2000
5. PRKCG mutation (SCA-14) causing a Ramsay Hunt phenotype;Visser;Mov Disord,2007
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