Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism

Annals of Neurology

Volumn 48, Issue 2, 2000, Pages 245-250

  Maruyama, Mieko ^a   Ikeuchi, Takeshi ^a   Saito, Masaaki ^a,b   Ishikawa, Atsushi ^d   Yuasa, Tatsuhiko ^e   Tanaka, Hajime ^c   Hayashi, Shintaro ^a   Wakabayashi, Koichi ^a   Takahashi, Hitoshi ^a   Tsuji, Shoji ^a  

^a NIIGATA UNIVERSITY   (Japan)

^b Nishi Niigata Central Hospital   (Japan)

^c Shinrakuen Hospital   (Japan)

^d Nishi Ojiya National Hospital   (Japan)

^e National Center for Global Health and Medicine   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE INHERITANCE; CLINICAL ARTICLE; DELETION MUTANT; FEMALE; GENE DOSAGE; GENETIC ANALYSIS; GENOTYPE; HUMAN; HUMAN CELL; MALE; MISSENSE MUTATION; NONSENSE MUTATION; ONSET AGE; PARKINSONISM; POINT MUTATION; PRIORITY JOURNAL; SCHOOL CHILD; SEQUENCE ANALYSIS;

ADOLESCENT; ADULT; CHILD; CODON, NONSENSE; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENE DELETION; GENE DOSAGE; GENES, DOMINANT; GENOTYPE; HUMAN; MALE; MUTATION; MUTATION, MISSENSE; PARKINSONIAN DISORDERS; PEDIGREE; PHENOTYPE; PROTEINS; SUPPORT, NON-U.S. GOV'T;

EID: 0033868381     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(200008)48:2<245::AID-ANA15>3.0.CO;2-2     Document Type: Article

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