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Q47595619-BEFE7FDB-6F5B-4283-8F8D-7BD865ACB51A
Q47595619-BEFE7FDB-6F5B-4283-8F8D-7BD865ACB51A
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http://www.wikidata.org/entity/statement/Q47595619-BEFE7FDB-6F5B-4283-8F8D-7BD865ACB51A
Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death.
P2860
Q47595619-BEFE7FDB-6F5B-4283-8F8D-7BD865ACB51A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47595619-BEFE7FDB-6F5B-4283-8F8D-7BD865ACB51A
rank
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wasDerivedFrom
a24642f74792ac67d9686875bda5b223bc78ccae
P2860
Cardiac sodium channel mutations: why so many phenotypes?