3-methylglutaric acid
National Institutes of Health
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
X-linked cardioskeletal myopathy, neutropenia and abnormal mitochondria (MIM 302060) (synonyms: Barth syndrome, 3…
Hereditary optic atrophy is a generic term that refers to a heterogeneous group of genetic disorders for which several modes of…
3-Methylglutaconic aciduria type I is an autosomal recessive disorder clinically characterized by various symptoms ranging from…
Type III 3-methylglutaconic aciduria (MGA) (MIM 258501) is a neuro-ophthalmologic syndrome that consists of early-onset bilateral…