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Methylglutaconyl-CoA hydratase / Tafazzin / Barth syndrome / 3-Methylglutaconic acid / Inborn error of metabolism / Biology / 3-Methylglutaconic aciduria / OPA3
Date: 2011-01-16 02:53:01
Methylglutaconyl-CoA hydratase
Tafazzin
Barth syndrome
3-Methylglutaconic acid
Inborn error of metabolism
Biology
3-Methylglutaconic aciduria
OPA3

Disease Name: 3-METHYLGLUTACONIC ACIDURIA TYPE II (X-LINKED CARIOSKELATAL MYOPATHY, NEUTROPENIA & ABNORMAL MITOCHONDRIA) (BARTH SYNDROME; MGA, TYPE II)

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