Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease
about
Targeted deletion of both thymidine phosphorylase and uridine phosphorylase and consequent disorders in miceA biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of QuebecPyruvate dehydrogenase deficiency due to a 20-bp deletion in exon II of the pyruvate dehydrogenase (PDH) E1 alpha gene.Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene.Cytochrome c oxidase dysfunction in oxidative stress.
P2860
Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease
description
1987 nî lūn-bûn
@nan
1987 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease
@ast
Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease
@en
type
label
Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease
@ast
Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease
@en
prefLabel
Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease
@ast
Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease
@en
P2093
P2860
P1476
Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease
@en
P2093
P2860
P304
P407
P577
1987-10-01T00:00:00Z