Spinocerebellar ataxia with mental retardation (SCA13)

Cerebellum

Volumn 4, Issue 1, 2005, Pages 43-46

  Stevanin, Giovanni ^a   Durr, Alexandra ^a   Benammar, Nawal ^a   Brice, Alexis ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

Chromosome mapping; Linkage (genetics); Mental retardation; Spinocerebellar ataxias; Spinocerebellar degenerations

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BASE PAIRING; CHROMOSOME 19Q; CHROMOSOME MAP; CLINICAL FEATURE; FRANCE; GENE IDENTIFICATION; GENE MAPPING; HUMAN; LINKAGE ANALYSIS; MENTAL DEFICIENCY; ONSET AGE; PRIORITY JOURNAL; SPINOCEREBELLAR DEGENERATION; SPNIOCEREBELLAR ATAXIA TYPE 13; SYMPTOM;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 19; DNA MUTATIONAL ANALYSIS; HUMANS; LINKAGE (GENETICS); MAGNETIC RESONANCE IMAGING; MENTAL RETARDATION; PEDIGREE; PHENOTYPE; SPINOCEREBELLAR ATAXIAS;

EID: 17844383743     PISSN: 14734222     EISSN: None     Source Type: Journal    
DOI: 10.1080/14734220510007923     Document Type: Article

References (20)

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