A study of six point mutation analysis of LRRK2 gene in Chinese mainland patients with Parkinson's disease

Neurological Sciences

Volumn 32, Issue 4, 2011, Pages 741-742

  Hu, Z X ^a   Peng, D T ^b   Cai, M ^a   Pu, J L ^a   Lei, X G ^a   Yin, X Z ^a   Ou Yang, Z Y ^a   Luo, W ^a   Zhang, B R ^a  

^a ZHEJIANG UNIVERSITY   (China)

^b BEIJING HOSPITAL   (China)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

ADULT; AGED; CHILD; CHINESE; CONTROLLED STUDY; DNA ISOLATION; ETHNICITY; EXON; FEMALE; GENE SEQUENCE; GENETIC VARIABILITY; HUMAN; LETTER; LEUCINE RICH REPEAT KINASE 2 GENE; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; MUTATOR GENE; ONSET AGE; PARKINSON DISEASE; POINT MUTATION; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SCHOOL CHILD;

ADOLESCENT; ADULT; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MIDDLE AGED; PARKINSON DISEASE; POINT MUTATION; PROTEIN-SERINE-THREONINE KINASES; RISK FACTORS; YOUNG ADULT;

EID: 80053967546     PISSN: 15901874     EISSN: 15903478     Source Type: Journal    
DOI: 10.1007/s10072-010-0453-8     Document Type: Letter

References (5)

1. Thomas G (2009) Molecular pathogenesis of Parkinson disease: insights from genetic studies. Expert Rev Mol Med. doi:10.1077/S1462399409001148
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