Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene.
about
Mitochondrial cytochrome c oxidase deficiencyThe adaptive evolution of the mammalian mitochondrial genomeDe novo mtDNA point mutations are common and have a low recurrence risk.Adaptation of the Mitochondrial Genome in Cephalopods: Enhancing Proton Translocation Channels and the Subunit Interactions.Mitochondrial mutations are associated with atherosclerotic lesions in the human aortaAssociation of mitochondrial genetic variation with carotid atherosclerosisAlteration of structure and function of ATP synthase and cytochrome c oxidase by lack of Fo-a and Cox3 subunits caused by mitochondrial DNA 9205delTA mutation.
P2860
Q26769015-B061F7BA-49D8-47E0-8A2D-0C42F8356686Q28754651-AF65E3D7-111B-45D3-8FD7-3F2470CB49F4Q33886230-F94C83F7-80A3-4BA1-8F0C-1F13EAED086BQ35748941-A90FB290-E41E-41D1-BC23-C5A614C9B5FCQ36246980-F3127858-C66E-43A9-8500-CAA216D32CC5Q36997420-3E6BE5C6-FBAA-4500-8EF0-F6A045AE056FQ38920032-B12DE6CB-A3F6-46F2-AC77-B51AAE5794CB
P2860
Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Childhood onset mitochondrial ...... cytochrome c oxidase III gene.
@en
Childhood onset mitochondrial ...... cytochrome c oxidase III gene.
@nl
type
label
Childhood onset mitochondrial ...... cytochrome c oxidase III gene.
@en
Childhood onset mitochondrial ...... cytochrome c oxidase III gene.
@nl
prefLabel
Childhood onset mitochondrial ...... cytochrome c oxidase III gene.
@en
Childhood onset mitochondrial ...... cytochrome c oxidase III gene.
@nl
P2093
P356
P1476
Childhood onset mitochondrial ...... cytochrome c oxidase III gene.
@en
P2093
C Schröder
H Lochmüller
J Müller-Höcker
K D Gerbitz
P J Oefner
P304
P356
10.1136/JMG.39.11.812
P407
P577
2002-11-01T00:00:00Z