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Q35998816-A0CF437E-F619-4E37-BEC2-028ECA0A9A3E
Q35998816-A0CF437E-F619-4E37-BEC2-028ECA0A9A3E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35998816-A0CF437E-F619-4E37-BEC2-028ECA0A9A3E
Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy
P2860
Q35998816-A0CF437E-F619-4E37-BEC2-028ECA0A9A3E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35998816-A0CF437E-F619-4E37-BEC2-028ECA0A9A3E
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Statement
wasDerivedFrom
ba441a646f708f62cf80136936851a5569a3368b
P2860
A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism.