Spinocerebellar Ataxia Type 14 Caused by a Mutation in Protein Kinase C γ

Archives of Neurology

Volumn 60, Issue 12, 2003, Pages 1749-1751

  Yabe, Ichiro ^a   Sasaki, Hidenao ^a   Chen, Dong Hui ^b   Raskind, Wendy H ^b   Bird, Thomas D ^b   Yamashita, Isao ^c   Tsuji, Shoji ^d   Kikuchi, Seiji ^a   Tashiro, Kunio ^a  

^a HOKKAIDO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b UNIVERSITY OF WASHINGTON   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; DNA; GLUTAMINE; PROTEIN KINASE C; PROTEIN KINASE C GAMMA;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 19Q; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DEGENERATIVE DISEASE; DISEASE CLASSIFICATION; DNA DETERMINATION; EXON; FEMALE; GENE FREQUENCY; GENE IDENTIFICATION; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; HUMAN; JAPAN; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; MYOCLONUS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SPINOCEREBELLAR DEGENERATION;

ADULT; AGED; ARGININE; BASE SEQUENCE; CASE-CONTROL STUDIES; GLYCINE; HETEROZYGOTE; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; PEDIGREE; PROTEIN KINASE C; SPINOCEREBELLAR ATAXIAS;

EID: 0346754906     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.60.12.1749     Document Type: Article

References (12)

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