OPA3

#	Item
1	Disease Name: 3-METHYLGLUTACONIC ACIDURIA TYPE II (X-LINKED CARIOSKELATAL MYOPATHY, NEUTROPENIA & ABNORMAL MITOCHONDRIA) (BARTH SYNDROME; MGA, TYPE II) Add to Reading List Source URL: public.health.oregon.gov Language: English - 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
2	Title: MEGDEL Syndrome GeneReview – Table 3 with Additional Protein Information Authors: Wortmann SB, De Brouwer APM, Wevers RA, Morava E Date: April 2014 Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English 3-Methylglutaconic aciduria Methylglutaconyl-CoA hydratase Tafazzin Barth syndrome Mitochondrion Cardiolipin OPA3 Dysmorphic feature Phosphatidylglycerol Biology Membrane biology Phospholipids