Camptocormia, axial dystonia, and parkinsonism: Phenotypic heterogeneity of a parkin mutation

Neurology

Volumn 60, Issue 8, 2003, Pages 1393-1394

  Inzelberg, Rivca ^a,b   Hattori, N ^c   Nisipeanu, P ^a   Abo Mouch, S ^a   Blumen, S C ^a,b   Carasso, R L ^a   Mizuno, Y ^c  

^a HILLEL YAFFE MEDICAL CENTER   (Israel)

^b TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^c JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; LEVODOPA; PARKIN;

ADULT; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONSANGUINITY; DISEASE COURSE; DISEASE DURATION; DNA EXTRACTION; DYSTONIA; EXON; FEMALE; GENE DELETION; GENE EXPRESSION; GENE MUTATION; GENE SEQUENCE; GENOTYPE; HUMAN; LABORATORY TEST; MALE; MOLECULAR BIOLOGY; ONSET AGE; PARKINSONISM; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RACE DIFFERENCE; RESTRICTION MAPPING; SIBLING; TREATMENT OUTCOME;

EID: 0037461313     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000055809.71968.87     Document Type: Article

References (7)

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3. Nisipeanu P, Inzelberg R, Blumen SC, et al. Autosomal recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of parkin gene. Neurology 1999;53:1602-1604.
4. Nisipeanu P, Inzelberg R, Abo Mouch S, et al. Parkin gene causing benign autosomal recessive juvenile parkinsonism. Neurology 2001;56:1573-1575.
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