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Molecular basis of 3‐ketothiolase deficiency: Detection of gene mutations and expression of mutant cDNAs of mitochondrial acetoacetyl‐CoA thiolase
Author(s) -
Fukao T.,
Yamaguchi S.,
Wakazono A.,
Okamoto H.,
Orii T.,
Osumi T.,
Hashimoto T.
Publication year - 1992
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/bf01800027
Subject(s) - thiolase , mutant , genetics , gene , biology , mutation , microbiology and biotechnology , human genetics , gene expression , mitochondrial dna , peroxisome