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Q43663646-149454DB-D926-47E0-9CE8-26F79D3B70EA
Q43663646-149454DB-D926-47E0-9CE8-26F79D3B70EA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43663646-149454DB-D926-47E0-9CE8-26F79D3B70EA
Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes.
P2860
Q43663646-149454DB-D926-47E0-9CE8-26F79D3B70EA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43663646-149454DB-D926-47E0-9CE8-26F79D3B70EA
rank
NormalRank
type
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Statement
wasDerivedFrom
3c079abe2111ba24410d0a2ff6e028595068bee2
P2860
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.