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Q55670918-CCC65216-EA9A-4D7D-82FF-838D605EE4F1
Q55670918-CCC65216-EA9A-4D7D-82FF-838D605EE4F1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55670918-CCC65216-EA9A-4D7D-82FF-838D605EE4F1
Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients
P2860
Q55670918-CCC65216-EA9A-4D7D-82FF-838D605EE4F1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55670918-CCC65216-EA9A-4D7D-82FF-838D605EE4F1
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wasDerivedFrom
7149b16ae0b84db349c995c46f558b1650b886d5
P2860
3-Hydroxy-3-methylglutaryl CoA lyase (HL): mouse and human HL gene (HMGCL) cloning and detection of large gene deletions in two unrelated HL-deficient patients.