Identification of 46 CAG repeats within PPP2R2B as probably the shortest pathogenic allele for SCA12
Author:
Funder
National Natural Science Foundation
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference12 articles.
1. Spinocerebellar ataxias type 8, 12, and 17 and dentatorubro-pallidoluysian atrophy in Czech ataxic patients;Musova;Cerebellum,2013
2. Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12;Holmes;Nat Genet,1999
3. Clinical features and classification of inherited ataxias;Harding;Adv Neurol,1993
4. SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family;Fujigasaki;Ann Neurol,2001
5. Molecular and clinical correlation in five Indian families with spinocerebellar ataxia 12;Srivastava;Ann Neurol,2001
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