Mutation analysis for DJ-1 in sporadic and familial parkinsonism: Screening strategy in parkinsonism

Neuroscience Letters

Volumn 455, Issue 3, 2009, Pages 159-161

  Tomiyama, Hiroyuki ^a   Li, Yuanzhe ^a   Yoshino, Hiroyo ^a   Mizuno, Yoshikuni ^a   Kubo, Shin ichiro ^a   Toda, Tatsushi ^b   Hattori, Nobutaka ^a  

^a JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b OSAKA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

1p36; Autosomal recessive parkinsonism; DJ 1; PARK7; Parkinson's disease; Sporadic parkinsonism

Indexed keywords

DJ 1 PROTEIN; PARKIN;

ADOLESCENT; ADULT; AGED; ARTICLE; ATP13A2 GENE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CONSANGUINITY; ETHNICITY; EXON; FAMILY HISTORY; FEMALE; GENE; GENE MUTATION; GENETIC SCREENING; HAPLOTYPE; HOMOZYGOSITY; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; ONSET AGE; PARK2 GENE; PARKINSONISM; PINK1 GENE; PREVALENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

CHROMOSOME DISORDERS; COHORT STUDIES; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, RECESSIVE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HUMANS; INHERITANCE PATTERNS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MALE; MUTATION; ONCOGENE PROTEINS; PARKINSON DISEASE; PROTEIN KINASES; PROTON-TRANSLOCATING ATPASES; UBIQUITIN-PROTEIN LIGASES;

EID: 64049087582     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2009.03.033     Document Type: Article

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