Molecular defects in the E1 alpha subunit of the branched-chain alpha-ketoacid dehydrogenase complex that cause maple syrup urine disease
about
Post-Translational Modifications of Cardiac Mitochondrial Proteins in Cardiovascular Disease: Not Lost in TranslationBranched-chain amino acids in metabolic signalling and insulin resistanceDevelopmental Defects of Caenorhabditis elegans Lacking Branched-chain α-Ketoacid Dehydrogenase Are Mainly Caused by Monomethyl Branched-chain Fatty Acid Deficiency.Mitochondrial protein phosphorylation as a regulatory modality: implications for mitochondrial dysfunction in heart failure.A simple method to confirm and size deletion, duplication, and insertion mutations detected by sequence analysis.
P2860
Molecular defects in the E1 alpha subunit of the branched-chain alpha-ketoacid dehydrogenase complex that cause maple syrup urine disease
description
1991 nî lūn-bûn
@nan
1991 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Molecular defects in the E1 al ...... ause maple syrup urine disease
@ast
Molecular defects in the E1 al ...... ause maple syrup urine disease
@en
Molecular defects in the E1 al ...... ause maple syrup urine disease
@nl
type
label
Molecular defects in the E1 al ...... ause maple syrup urine disease
@ast
Molecular defects in the E1 al ...... ause maple syrup urine disease
@en
Molecular defects in the E1 al ...... ause maple syrup urine disease
@nl
prefLabel
Molecular defects in the E1 al ...... ause maple syrup urine disease
@ast
Molecular defects in the E1 al ...... ause maple syrup urine disease
@en
Molecular defects in the E1 al ...... ause maple syrup urine disease
@nl
P2093
P1476
Molecular defects in the E1 al ...... ause maple syrup urine disease
@en
P2093
P407
P577
1991-02-01T00:00:00Z