Human Biotin-Containing Subunit of 3-Methylcrotonyl-CoA Carboxylase Gene (MCCA): cDNA Sequence, Genomic Organization, Localization to Chromosomal Band 3q27, and Expression-Reference-Cited by-同舟云学术

Human Biotin-Containing Subunit of 3-Methylcrotonyl-CoA Carboxylase Gene (MCCA): cDNA Sequence, Genomic Organization, Localization to Chromosomal Band 3q27, and Expression

Published:2001-03 Issue:2 Volume:72 Page:145-152
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Obata Keiko,Fukuda Takayuki,Morishita Riyo,Abe Shunnosuke,Asakawa Shuichi,Yamaguchi Seiji,Yoshino Makoto,Ihara Kenji,Murayama Keiko,Shigemoto Kazuhiro,Shimizu Nobuyoshi,Kondo Ikuko

Publisher

Elsevier BV

Subject

Genetics

Reference24 articles.

1. Isolated biotin-resistant deficiency of 3-methylcrotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome;Bannwart;J. Inherit. Metab. Dis.,1992

2. Familial hypotonia of childhood caused by isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency;Elpeleg;J. Pediatr.,1992

3. Massive excretion of 2-oxoglutaric acid and 3-hydroxyisovaleric acid in a patient with a deficiency of 3-methylcrotonyl-CoA carboxylase;Finnie;Clin. Chim. Acta,1976

4. 3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their children;Gibson;J. Pediatr.,1998

5. Survey of amino-terminal proteolytic cleavage sites in mitochondrial precursor proteins: Leader peptides cleaved by two matrix proteases share a three-amino acid motif;Hendrick;Proc. Natl. Acad. Sci USA,1989

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