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Volumn 35, Issue 3, 2014, Pages 727.e5-727.e7
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Systematic mutational analysis of FBXO7 in a Parkinson's disease population from southern Spain
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Author keywords
Early onset; FBXO7; Mutational analysis; Parkinson's disease; Parkinsonism; Pyramidal signs; Variants
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Indexed keywords
AMINO ACID SUBSTITUTION;
ARTICLE;
COMPUTER MODEL;
CONTROLLED STUDY;
EXON;
FBXO7 GENE;
GENE DELETION;
GENE DUPLICATION;
GENE FREQUENCY;
GENE MUTATION;
GENETIC VARIABILITY;
HETEROZYGOSITY;
HUMAN;
INTRON;
MAJOR CLINICAL STUDY;
MISSENSE MUTATION;
MUTATIONAL ANALYSIS;
PARKINSON DISEASE;
PATHOGENESIS;
PRIORITY JOURNAL;
RNA SPLICING;
SINGLE NUCLEOTIDE POLYMORPHISM;
SPAIN;
EARLY-ONSET;
FBXO7;
MUTATIONAL ANALYSIS;
PARKINSON'S DISEASE;
PARKINSONISM;
PYRAMIDAL SIGNS;
VARIANTS;
AGE OF ONSET;
DNA MUTATIONAL ANALYSIS;
F-BOX PROTEINS;
HUMANS;
MUTATION;
PARKINSON DISEASE;
SPAIN;
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EID: 84889587259
PISSN: 01974580
EISSN: 15581497
Source Type: Journal
DOI: 10.1016/j.neurobiolaging.2013.09.011 Document Type: Article |
Times cited : (11)
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References (0)
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