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Volumn 18, Issue 7, 2013, Pages 739-
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Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics
a b a a a a a a a a c b b d e f e g,h i j more.. |
Author keywords
[No Author keywords available]
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Indexed keywords
BRAIN DISEASE;
BRAIN SIZE;
EXOME;
GENE FUNCTION;
GENE SEQUENCE;
GENETIC IDENTIFICATION;
GENETIC VARIABILITY;
GENOTYPE;
HUMAN;
MILD COGNITIVE IMPAIRMENT;
NERVE DEGENERATION;
NEUROIMAGING;
NOTE;
PRIORITY JOURNAL;
QUANTITATIVE TRAIT;
ATROPHY;
EXOME;
GENOME-WIDE ASSOCIATION STUDY;
HIPPOCAMPUS;
HUMANS;
MILD COGNITIVE IMPAIRMENT;
NEUROIMAGING;
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EID: 84879398862
PISSN: 13594184
EISSN: 14765578
Source Type: Journal
DOI: 10.1038/mp.2013.81 Document Type: Note |
Times cited : (9)
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References (0)
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