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NDUFV1 gene

Known as: NDUFV1, NADH-UBIQUINONE OXIDOREDUCTASE FLAVOPROTEIN 1, NADH:ubiquinone oxidoreductase core subunit V1 
This gene plays a role in cellular respiration.
National Institutes of Health

Related topics

Related topics

6 relations
Cell RespirationNDUFS5 geneNDUFV2 geneNDUFV3 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Phenotype of NDUFV1-related Disease
2018
2018
Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations
2017
2017
[Clinical and genetic characteristics of children with Leigh syndrome].
Objective: To investigate the clinically and genetic characteristics of children with Leigh syndrome. Method: Patients with… 
2013
2013
Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosis
Infantile bilateral striatal necrosis (IBSN) includes a heterogeneous group of disorders, characterized by symmetrical… 
2012
2012
Episodic Leukoencephalopathy Due to Novel Mitochondrial Complex I NDUFV1 Gene Mutations (P02.172)
Objective: To report a child with clinically episodic leukoencephalopathy due to two novel mutations in mitochondrial Complex I… 
2007
2007
Clinical complete long-term remission of a patient with metastatic malignant melanoma under therapy with indisulam (E7070).
The objective of this study is to report on long-term survival of a patient with metastatic melanoma treated with indisulam… 
2005
2005
Unusual features of mitochondrial degeneration in skeletal muscle of patients with nuclear complex I mutation
We examined the histopathological finding in muscle of four patients with known nuclear mutations of complex I subunits. No… 
Highly Cited
2003
Highly Cited
2003
Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation…
Complex I deficiency, the most common cause of mitochondrial disorders, accounts for a variety of clinical symptoms and its… 
2002
2002
New nuclear encoded mitochondrial mutation illustrates pitfalls in prenatal diagnosis by biochemical methods.
A frequent etiology of congenital lactic acidosis is disturbed mitochondrial energy metabolism. Affected children generally… 
1999
1999
The structure of the human NDUFV1 gene encoding the 51-kDa subunit of mitochondrial complex I
Abstract. The genomic organization of the human 51-kDa subunit gene (NDUFV1) on human Chromosome (Chr) 11q13 was determined. The… 
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