Exploration of CAG triplet repeat in nontranslated region of SCA12 gene

Spinocerebellar Ataxia Type 12 was not Found in Korean Parkinsonian Patients

(2014) Jin Whan Cho et al.   CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES

Role of Dynamic and Mitochondrial Mutations in Neurodegenerative Diseases with Ataxia: Lower Repeats and LNAs at Multiple Loci as Alternative Pathogenesis

(2014) Waseem Gul Lone et al.   JOURNAL OF MOLECULAR NEUROSCIENCE

Spinocerebellar ataxias: An example of the challenges associated with genetic databases for dynamic mutations

(2012) Joanne E. Martindale et al.   HUMAN MUTATION

Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia

(2010) Alessandro Brussino et al.   MOVEMENT DISORDERS

SCA-LSVD: A repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias

(2009) Mohammed Faruq et al.   HUMAN MUTATION

Utilizing linkage disequilibrium information from Indian Genome Variation Database for mapping mutations: SCA12 case study

(2009) Samira Bahl et al.   JOURNAL OF GENETICS

PPP2R2BCAG repeat length in the Han Chinese in Taiwan: Association analyses in neurological and psychiatric disorders and potential functional implications

(2008) Chiung-Mei Chen et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS