Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Mitochondrial ATP synthase deficiency due to 8993T > G mutation on ATP6 gene].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 1 Jul 2011

Ma Yan-yan, Wu Tong-fei, Liu Yu-peng

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Infant
Share to Mitochondrial Proton-Translocating ATPases
Share to Mutation

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 22088191

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Mitochondrial ATP synthase deficiency due to 8993T > G mutation on ATP6 gene].PMID 22088191Read ↗

[Hereditary disorders of mitochondrial ATP synthase].Semantic proximity Read ↗

[Complex V (ATP synthase) deficiency].Semantic proximity Read ↗

[Diseases caused by mutations in mitochondrial DNA].Semantic proximity Read ↗

[A novel mutation in ATP7B gene associated with severe neurological impairment in Wilson's disease].Semantic proximity Read ↗

Analysis of MT-ATP8 gene variants reported in patients by modeling in silico and in yeast model organism.Semantic proximity Read ↗

[Complex I deficiency due to NDUFS8 gene mutation].Semantic proximity Read ↗

A novel splice-site mutation in ATP6V0A4 gene in two brothers with distal renal tubular acidosis from a consanguineous Tunisian family.Semantic proximity Read ↗

Clinical spectrum of disease associated with ATP1A3 mutationsSemantic proximity Read ↗

[Gene mutation in mitochondrial DNA disease].Semantic proximity Read ↗

Defective mitochondrial ATPase due to rare mtDNA m.8969G>A mutation-causing lactic acidosis, intellectual disability, and poor growth.Semantic proximity Read ↗

[A8344G mitochondrial DNA mutation observed in two generations].Semantic proximity Read ↗

Nuclear genetic defects of mitochondrial ATP synthase.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.