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Q38616789-224D5543-F6D3-4E5B-A794-1D893051C938
Q38616789-224D5543-F6D3-4E5B-A794-1D893051C938
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38616789-224D5543-F6D3-4E5B-A794-1D893051C938
Genetic studies in intellectual disability and related disorders.
P2860
Q38616789-224D5543-F6D3-4E5B-A794-1D893051C938
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38616789-224D5543-F6D3-4E5B-A794-1D893051C938
rank
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type
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Statement
wasDerivedFrom
c14e43f68b2aaf8fa85ccf5495b82f8c985d64be
P2860
SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain.