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1
Q33847202-7CD26ECA-78AA-4A86-8355-2F76623D3865
Q33847202-7CD26ECA-78AA-4A86-8355-2F76623D3865
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http://www.wikidata.org/entity/statement/Q33847202-7CD26ECA-78AA-4A86-8355-2F76623D3865
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
P2860
Q33847202-7CD26ECA-78AA-4A86-8355-2F76623D3865
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33847202-7CD26ECA-78AA-4A86-8355-2F76623D3865
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wasDerivedFrom
bc0f280ba800b72821ce1e91dfd67bd19f3a017a
P2860
A genome-wide investigation of SNPs and CNVs in schizophrenia.