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Volumn 40, Issue 1, 1995, Pages 131-143

Spinocerebellar ataxia 1 (SCA1) in the Japanese: Analysis of CAG trinucleitide repeat expansion and instability of the repeat for paternal transmission

(9) Suzuki, Yoshihiro a Sasaki, Hidenao a Wakisaka, Akemi a Takada, Akio a Yoshiki, Takashi a Iwabuchi, Kiyoshi b Tashiro, Kunio a Fukazawa, Toshiyuki c Hamada, Takeshi c

a HOKKAIDO UNIVERSITY (Japan)

b KANAGAWA REHABILITATION CENTER (Japan)

c Hokuyukai Neurology Hospital (Japan)

Author keywords

CAG repeat; hereditary ataxia; olivopontocerebellar atrophy; spinocerebellar ataxia 1 (SCA1)

Indexed keywords

DNA; TRINUCLEOTIDE;

ADOLESCENT; ADULT; ARTICLE; CEREBELLAR ATAXIA; CHROMOSOME 6P; CONTROLLED STUDY; DNA SEQUENCE; FEMALE; GENE LOCATION; GENE SEGREGATION; GENETIC LINKAGE; GENETIC STABILITY; HAPLOTYPE; HEREDITARY ATAXIA; HUMAN; INHERITANCE; JAPAN; MAJOR CLINICAL STUDY; MALE; OLIVOPONTOCEREBELLAR ATROPHY; ONSET AGE; PEDIGREE; SPINOCEREBELLAR DEGENERATION;

ADOLESCENT; ADULT; ALLELES; BASE SEQUENCE; FEMALE; HUMAN; JAPAN; MALE; MIDDLE AGE; MOLECULAR SEQUENCE DATA; MONGOLOID RACE; REPETITIVE SEQUENCES, NUCLEIC ACID; SEX FACTORS; SPINOCEREBELLAR DEGENERATIONS; SUPPORT, NON-U.S. GOV'T;

EID: 0028938117 PISSN: 09168478 EISSN: 1435232X Source Type: Journal
DOI: 10.1007/BF01874077 Document Type: Article

Times cited : (13)

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