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Q34682335-F6C1DF59-EEBD-4240-B4CE-E77D163DE118
Q34682335-F6C1DF59-EEBD-4240-B4CE-E77D163DE118
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34682335-F6C1DF59-EEBD-4240-B4CE-E77D163DE118
Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autism
P2860
Q34682335-F6C1DF59-EEBD-4240-B4CE-E77D163DE118
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34682335-F6C1DF59-EEBD-4240-B4CE-E77D163DE118
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wasDerivedFrom
b61137d3a1b078a4073aaa87619c3e6423f54c2f
P2860
Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.