3-methylbutyrylcarnitine and Acute-Disease

3-methylbutyrylcarnitine has been researched along with Acute-Disease* in 1 studies

Other Studies

1 other study(ies) available for 3-methylbutyrylcarnitine and Acute-Disease

Article	Year
Genotype and phenotype characterization in a Spanish cohort with isovaleric acidemia. Journal of human genetics, 2017, Volume: 62, Issue:3 Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Asymptomatic Diseases; Carnitine; Child; Child, Preschool; Chronic Disease; Creatinine; Female; Fibroblasts; Gene Expression; Genetic Association Studies; Genotype; Glycine; Hemiterpenes; Humans; Infant; Infant, Newborn; Isovaleryl-CoA Dehydrogenase; Male; Mutation; Neonatal Screening; Pentanoic Acids; Phenotype; Prevalence; Spain	2017

Article

Year

Genotype and phenotype characterization in a Spanish cohort with isovaleric acidemia.

Journal of human genetics, 2017, Volume: 62, Issue:3

Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Asymptomatic Diseases; Carnitine; Child; Child, Preschool; Chronic Disease; Creatinine; Female; Fibroblasts; Gene Expression; Genetic Association Studies; Genotype; Glycine; Hemiterpenes; Humans; Infant; Infant, Newborn; Isovaleryl-CoA Dehydrogenase; Male; Mutation; Neonatal Screening; Pentanoic Acids; Phenotype; Prevalence; Spain

2017