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Q58699948-CE719B52-DB1B-4432-99AD-54879841E260
Q58699948-CE719B52-DB1B-4432-99AD-54879841E260
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58699948-CE719B52-DB1B-4432-99AD-54879841E260
Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports
P2860
Q58699948-CE719B52-DB1B-4432-99AD-54879841E260
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58699948-CE719B52-DB1B-4432-99AD-54879841E260
rank
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Statement
wasDerivedFrom
b679e5d7182484d59b6dada377e5e7f92967b9cc
P2860
Identification of 16 new disease-causing mutations in the CPT2 gene resulting in carnitine palmitoyltransferase II deficiency