SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family

Annals of Neurology

Volumn 49, Issue 1, 2001, Pages 117-121

  Fujigasaki, Hiroto ^a   Verma, Ishwar C ^a   Camuzat, Agnès ^b   Margolis, Russell L ^b   Zander, Cecilia ^b   Lebre, Anne Sophie ^b   Jamot, Laure ^c   Saxena, Renu ^c   Anand, Ish ^d   Holmes, Susan E ^b   Ross, Christopher A ^c   Dürr, Alexandra ^c   Brice, Alexis ^a,d  

^a INSERM   (France)

^b SIR GANGA RAM HOSPITAL   (India)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PHOSPHOPROTEIN PHOSPHATASE 2A; PROTEIN PPP2R2B; PROTEIN SCA12; UNCLASSIFIED DRUG;

ADULT; AGED; ALLELE; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CEREBELLAR ATAXIA; CONTROLLED STUDY; GENE LOCUS; GENE MUTATION; HUMAN; INDIA; MAJOR CLINICAL STUDY; NUCLEOTIDE REPEAT; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SPINOCEREBELLAR DEGENERATION;

ADULT; AGED; ALLELES; CEREBELLAR ATAXIA; FEMALE; FRANCE; HUMANS; INDIA; MALE; MIDDLE AGED; PEDIGREE; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 0035115573     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(200101)49:1<117::AID-ANA19>3.0.CO;2-G     Document Type: Article

References (16)

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