|
Volumn 21, Issue 8, 2006, Pages 1232-1235
|
Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease
a,b c d d d a d e f g h i h j k c a,b d a,b c more.. |
Author keywords
Dardarin; Italy; LRRK2; Mutation screening; Parkinson's disease
|
Indexed keywords
GENE PRODUCT;
LEUCINE RICH REPEAT KINASE 2;
UNCLASSIFIED DRUG;
ADOLESCENT;
ADULT;
AGED;
ARTICLE;
AUTOSOMAL DOMINANT INHERITANCE;
CONTROLLED STUDY;
DISEASE DURATION;
FAMILIAL DISEASE;
FAMILY HISTORY;
FEMALE;
GENE FREQUENCY;
GENE MUTATION;
GENOTYPE;
HAPLOTYPE;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
HUMAN;
ITALY;
MAJOR CLINICAL STUDY;
MALE;
ONSET AGE;
PARKINSON DISEASE;
PHENOTYPE;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
SINGLE NUCLEOTIDE POLYMORPHISM;
AMINO ACID SUBSTITUTION;
FEMALE;
GENE FREQUENCY;
HETEROZYGOTE DETECTION;
HUMANS;
ITALY;
MALE;
MUTATION;
PARKINSON DISEASE;
PHENOTYPE;
PROTEIN-SERINE-THREONINE KINASES;
|
EID: 33748347105
PISSN: 08853185
EISSN: 15318257
Source Type: Journal
DOI: 10.1002/mds.20890 Document Type: Article |
Times cited : (25)
|
References (10)
|