Alteration 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.
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Novel two-step derivation method for the synchronous analysis of inherited metabolic disorders using urine.Stable nuclear expression of ATP8 and ATP6 genes rescues a mtDNA Complex V null mutantTo unite or divide: mitochondrial dynamics in the murine outer retina that preceded age related photoreceptor loss.ATP Synthase Diseases of Mitochondrial Genetic Origin.
P2860
Alteration 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.
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2015 nî lūn-bûn
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Alteration of structure and fu ...... ndrial DNA 9205delTA mutation.
@en
type
label
Alteration of structure and fu ...... ndrial DNA 9205delTA mutation.
@en
prefLabel
Alteration of structure and fu ...... ndrial DNA 9205delTA mutation.
@en
P2093
P2860
P50
P356
P1433
P1476
Alteration of structure and fu ...... ndrial DNA 9205delTA mutation.
@en
P2093
Josef Houštěk
Kateřina Hejzlarová
Nikola Kovářová
Sara Seneca
Vilma Kaplanová
P2860
P304
P356
10.1042/BJ20141462
P407
P577
2015-03-01T00:00:00Z