LRRK2 P755L variant in sporadic Parkinson's disease

Journal of Human Genetics

Volumn 53, Issue 11-12, 2008, Pages 1012-1015

  Tomiyama, Hiroyuki ^a   Mizuta, Ikuko ^b,c   Li, Yuanzhe ^a   Funayama, Manabu ^a   Yoshino, Hiroyo ^a   Li, Lin ^a   Murata, Miho ^c,d   Yamamoto, Mitsutoshi ^c,e   Kubo, Shin Ichiro ^a   Mizuno, Yoshikuni ^a   Toda, Tatsushi ^b,c   Hattori, Nobutaka ^a,c  

^a JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b OSAKA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^c JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

^d NATIONAL INSTITUTE OF MENTAL HEALTH   (Japan)

^e KAGAWA PREFECTURAL CENTRAL HOSPITAL   (Japan)

Author keywords

Association study; Ethnic background; Genetics; Japanese; Leucine rich repeat kinase 2 (LRRK2); PARK8; Parkinson's disease; Polymorphism

Indexed keywords

LEUCINE RICH REPEAT KINASE 2;

ADULT; AGED; ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA SEQUENCE; ETHNICITY; EXON; FEMALE; GENE MUTATION; GENETIC VARIABILITY; HETEROZYGOSITY; HUMAN; JAPANESE; MAJOR CLINICAL STUDY; MALE; PARKINSON DISEASE; POPULATION GENETICS;

ADULT; AGED; AGED, 80 AND OVER; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; PARKINSON DISEASE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; PROTEIN-SERINE-THREONINE KINASES;

EID: 57349169297     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10038-008-0336-5     Document Type: Article

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