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3 methylglutaconic aciduria
Summary
General Info
Curated Studies
Most Correlated Studies
OMIM - Congenital disorder
OMIM - Disorder of amino acid metabolism
OMIM - Metabolic and Enzymatic Disorders
Cardiac gene expression in an inducible tafazzin shRNA knockdown mouse model of Barth syndrome
Dermal fibroblasts from pediatric patients with dilated cardiomyopathy with ataxia syndrome
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Mild form of 3-methylglutaconic aciduria type IV and mutation in the TMEM70 genes.
Exome sequencing identifies a new mutation in SERAC1 in a patient with 3-methylglutaconic aciduria.
Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-Methylglutaconic aci…
POLG mutation in a patient with cataracts, early-onset distal muscle weakness and atrophy, ovarian d…
Phenotypic heterogeneity in two siblings with 3-methylglutaconic aciduria type I caused by a novel i…
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There were no clinical trials for 3 methylglutaconic aciduria
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