Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6

National Medical Journal of China

Volumn 85, Issue 22, 2005, Pages 1538-1541

  Zhang, Yu Hu ^a   Tang, Bei Sha ^b   Guo, Ji Feng ^b   Xia, Kun ^b   Xu, Bo ^b   Cai, Fang ^b   Deng, Han Xiang ^b   Yan, Xin Xiang ^b   Chen, Tao ^b   Cao, Li ^b   Pan, Qian ^b   Long, Zhi Gao ^b  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b NONE

Author keywords

Chromosame abnormalities; Gene; Parkinsoniam disease; Parkinsoniam disorders

Indexed keywords

AMINO ACID; CYSTEINE; DNA; GENE PRODUCT; LEVODOPA; METHIONINE; PROTEIN PINK1; THREONINE; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHINESE; CHROMOSOME ANALYSIS; CHROMOSOME MUTATION; CIRCADIAN RHYTHM; CLINICAL FEATURE; DISEASE COURSE; DNA SEQUENCE; DYSKINESIA; EXON; FAMILY STUDY; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HYPERREFLEXIA; PARKINSONISM; PEDIGREE ANALYSIS; POINT MUTATION; POLYMERASE CHAIN REACTION; RESTRICTION MAPPING; SLEEP; STOP CODON;

ADOLESCENT; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; EXONS; FEMALE; HUMANS; MALE; MIDDLE AGED; PARKINSONIAN DISORDERS; PEDIGREE; POINT MUTATION; PROTEIN KINASES;

EID: 21244445382     PISSN: 03762491     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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