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Q35609938-818FA23D-E678-4564-A795-A4C3F63838E1
Q35609938-818FA23D-E678-4564-A795-A4C3F63838E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35609938-818FA23D-E678-4564-A795-A4C3F63838E1
Application of multiplex ligation-dependent probe amplification, and identification of a heterozygous Alu-associated deletion and a uniparental disomy of chromosome 1 in two patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
P921
Q35609938-818FA23D-E678-4564-A795-A4C3F63838E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35609938-818FA23D-E678-4564-A795-A4C3F63838E1
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type
BestRank
Statement
P921
3-hydroxy-3-methylglutaryl-CoA lyase deficiency