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Q34359072-C7837720-D92E-400C-9E54-DA0ACF32EF9E
Q34359072-C7837720-D92E-400C-9E54-DA0ACF32EF9E
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Statement
http://www.wikidata.org/entity/statement/Q34359072-C7837720-D92E-400C-9E54-DA0ACF32EF9E
Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome.
P2860
Q34359072-C7837720-D92E-400C-9E54-DA0ACF32EF9E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34359072-C7837720-D92E-400C-9E54-DA0ACF32EF9E
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Statement
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db59d44162d9f4ddabe6848d8b2df5f363a0d09b
P2860
The spectrum of SCN1A-related infantile epileptic encephalopathies.