Parkin dosage mutations in patients with early-onset sporadic and familial Parkinson's disease in Chinese: An independent pathogenic role

Brain Research

Volumn 1358, Issue , 2010, Pages 30-38

  Wang, Chaodong ^a   Ma, Huili ^a   Feng, Xiuli ^b   Xie, Shu ^b   Chan, Piu ^a,b  

^a CAPITAL MEDICAL UNIVERSITY   (China)

^b CHINESE NATIONAL HUMAN GENOME CENTER AT SHANGHAI   (China)

Author keywords

Autosomal recessive early onset parkinsonism; Dosage mutation; Early onset Parkinson's disease; Parkin

Indexed keywords

PARKIN;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BRADYKINESIA; CHINESE; CONTROLLED STUDY; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; DYSKINESIA; DYSTONIA; EXON; FAMILIAL DISEASE; FEMALE; GAIT DISORDER; GENE DELETION; GENE DOSAGE; GENE DUPLICATION; GENE FREQUENCY; GENE MUTATION; GENETIC RISK; HETEROZYGOTE; HOMOZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MALE; MULTIPLEX POLYMERASE CHAIN REACTION; MUTATIONAL ANALYSIS; NEUROPATHOLOGY; ONSET AGE; PARKINSON DISEASE; PRIORITY JOURNAL; REAL TIME POLYMERASE CHAIN REACTION; RISK ASSESSMENT; TREMOR;

ADULT; AGE OF ONSET; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; COHORT STUDIES; DNA MUTATIONAL ANALYSIS; EXONS; FAMILY HEALTH; FEMALE; GENE DOSAGE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MUTATION; PARKINSONIAN DISORDERS; STATISTICS AS TOPIC; UBIQUITIN-PROTEIN LIGASES;

EID: 77957374310     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2010.08.060     Document Type: Article

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