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Q48163958-100DC1A3-8674-4D7D-B010-C64C53E45A55
Q48163958-100DC1A3-8674-4D7D-B010-C64C53E45A55
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48163958-100DC1A3-8674-4D7D-B010-C64C53E45A55
Case-control pharmacogenetic study of HCN1/HCN2 variants and genetic generalized epilepsies.
P2860
Q48163958-100DC1A3-8674-4D7D-B010-C64C53E45A55
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48163958-100DC1A3-8674-4D7D-B010-C64C53E45A55
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
0e799ce92dbe60dbf3ff27ba107ccae5e9967a21
P2860
De novo mutations in HCN1 cause early infantile epileptic encephalopathy.