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Q24320280-13FEB40C-A9EA-4AAE-8BD2-5047A090297E
Q24320280-13FEB40C-A9EA-4AAE-8BD2-5047A090297E
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Statement
http://www.wikidata.org/entity/statement/Q24320280-13FEB40C-A9EA-4AAE-8BD2-5047A090297E
A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome
P2860
Q24320280-13FEB40C-A9EA-4AAE-8BD2-5047A090297E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24320280-13FEB40C-A9EA-4AAE-8BD2-5047A090297E
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wasDerivedFrom
222f9c8a7833abf99bec99f01fdb3be84c527a57
P2860
Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): mutations and polymorphisms in TRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor.