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Q37496956-B5F95111-E509-4B48-ACC9-A49CB90CB67D
Q37496956-B5F95111-E509-4B48-ACC9-A49CB90CB67D
BestRank
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http://www.wikidata.org/entity/statement/Q37496956-B5F95111-E509-4B48-ACC9-A49CB90CB67D
Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.
P2860
Q37496956-B5F95111-E509-4B48-ACC9-A49CB90CB67D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37496956-B5F95111-E509-4B48-ACC9-A49CB90CB67D
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wasDerivedFrom
d1c3b8c2db24fc5c6746a7ac240a04a7d8baed25
P2860
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome