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Volumn 19, Issue 11, 2013, Pages 1057-1060
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Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease
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Author keywords
Synuclein; Genetic etiology; Missense mutations; Parkinson's disease; SNCA gene
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Indexed keywords
ALPHA SYNUCLEIN;
ADULT;
AGED;
AMINO ACID SUBSTITUTION;
ARTICLE;
COMPUTER MODEL;
CONTROLLED STUDY;
EXON;
FAMILY HISTORY;
FEMALE;
GENE FREQUENCY;
GENE SEQUENCE;
GENETIC RISK;
GENETIC VARIABILITY;
HUMAN;
MAJOR CLINICAL STUDY;
MALE;
MICROARRAY ANALYSIS;
PARKINSON DISEASE;
PATHOGENICITY;
POINT MUTATION;
POLAND;
PRIORITY JOURNAL;
PROTEIN FUNCTION;
PROTEIN STRUCTURE;
SNCA GENE;
GENETIC ETIOLOGY;
MISSENSE MUTATIONS;
PARKINSON'S DISEASE;
SNCA GENE;
Α-SYNUCLEIN;
ADULT;
AGED;
AGED, 80 AND OVER;
ALPHA-SYNUCLEIN;
AMINO ACID SEQUENCE;
AMINO ACID SUBSTITUTION;
FEMALE;
GENETIC ASSOCIATION STUDIES;
HUMANS;
MALE;
MIDDLE AGED;
MOLECULAR SEQUENCE DATA;
MUTATION, MISSENSE;
PARKINSON DISEASE;
PEDIGREE;
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EID: 84886587005
PISSN: 13538020
EISSN: 18735126
Source Type: Journal
DOI: 10.1016/j.parkreldis.2013.07.011 Document Type: Article |
Times cited : (67)
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References (12)
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