The leucine rich repeat kinase 2 (LRRK2) G2019S substitution mutation : AAssociation with Parkinson disease, malignant melanoma and prevalence in ethnic groups in Israel

Journal of Neurology

Volumn 256, Issue 3, 2009, Pages 483-487

  Hassin Baer, Sharon ^a   Laitman, Yael ^b   Azizi, Esther ^a   Molchadski, Irena ^a   Galore Haskel, Gilli ^b   Barak, Frida ^c   Cohen, Oren S ^a   Friedman, Eitan ^b  

^a SHEBA MEDICAL CENTER   (Israel)

^b GERTNER INSTITUTE FOR EPIDEMIOLOGY AND HEALTH POLICY RESEARCH   (Israel)

^c BARZILAI MEDICAL CENTER   (Israel)

Author keywords

Germline mutation; Inherited predisposition; LRKK2 gene; Malignant melanoma; Parkinson's disease

Indexed keywords

LEUCINE RICH REPEAT KINASE 2;

AGED; ARTICLE; CANCER EPIDEMIOLOGY; CHI SQUARE TEST; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; ETHNIC GROUP; FEMALE; GEL ELECTROPHORESIS; GENETIC ASSOCIATION; GENOTYPE; HETEROZYGOTE; HUMAN; ISRAEL; MAJOR CLINICAL STUDY; MALE; MELANOMA; MISSENSE MUTATION; MUTATION; PARKINSON DISEASE; PREVALENCE; PRIORITY JOURNAL; RACE DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

AGE FACTORS; AGED; ETHNIC GROUPS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; ISRAEL; JEWS; MALE; MELANOMA; MIDDLE AGED; MUTATION, MISSENSE; PARKINSON DISEASE; PROTEIN-SERINE-THREONINE KINASES; SEQUENCE ANALYSIS, DNA;

EID: 65449160605     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-009-0117-x     Document Type: Article

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