PINK1 mutations in sporadic early-onset Parkinson's Disease

Movement Disorders

Volumn 21, Issue 6, 2006, Pages 789-793

  Tan, Eng King ^a,b,c   Yew, Kenneth ^b   Chua, Eva ^b   Puvan, K ^b,c   Shen, Hui ^b   Lee, Esther ^b   Puong, Kim Yoong ^b   Zhao, Yi ^b   Pavanni, Ratnagopal ^b,c   Wong, Meng Cheong ^b,c   Jamora, Dominic ^c   de Silva, Deidre ^b,c   Moe, Kyaw Thu ^b   Woon, Fung Peng ^b   Yuen, Yih ^b   Tan, Louis ^c  

^a Singapore Health Services   (Singapore)

^b SINGAPORE GENERAL HOSPITAL   (Singapore)

^c NATIONAL NEUROSCIENCE INSTITUTE   (Singapore)

Author keywords

Mutation; Parkinson's disease; PINK1; Restless legs syndrome

Indexed keywords

ALANINE; ALPHA SYNUCLEIN; LEVODOPA; NUCLEAR RECEPTOR RELATED FACTOR 1; PARKIN; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE; THREONINE;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; ASIAN; CHINESE; COHORT ANALYSIS; CONTROLLED STUDY; ETHNIC GROUP; EXON; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; INDIAN; INTRON; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NONSENSE MUTATION; PARKINSON DISEASE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DOMAIN; RESTLESS LEGS SYNDROME; RISK ASSESSMENT; SEQUENCE ANALYSIS;

ADULT; AGE OF ONSET; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; DNA PRIMERS; ETHNIC GROUPS; HETEROZYGOTE DETECTION; HOMOZYGOTE; HUMANS; MIDDLE AGED; MUTATION; PARKINSON DISEASE; PROTEIN KINASES; SINGAPORE;

EID: 33745845523     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.20810     Document Type: Article

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