Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency

author
dbId 70749
displayName Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency
journal Hum Mol Genet
pages 1299-306
pubMedIdentifier 11406611
schemaClass LiteratureReference
title Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency.
url http://www.ncbi.nlm.nih.gov/pubmed/11406611
volume 10
year 2001
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