(Q47757882)

English

The X-chromosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: tissue expression and mutation detection.

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scholarly article

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

The X-chromosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: tissue expression and mutation detection. (English)

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

author name string

J Loeffen

1

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

R Smeets

2

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

J Smeitink

3

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

W Ruitenbeek

4

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

A Janssen

5

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

E Mariman

6

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

R Sengers

7

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

F Trijbels

8

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

L van den Heuvel

9

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

publication date

1 June 1998

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

Journal of Inherited Metabolic Disease

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Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

21

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Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

210-215

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

3

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

https://scigraph.springernature.com/pub.10.1023/a:1005339332062

0 references

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Possible X linked congenital mitochondrial cardiomyopathy in three families

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary tyrosinemia type 1: novel missense, nonsense and splice consensus mutations in the human fumarylacetoacetate hydrolase gene; variability of the genotype-phenotype relationship

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation, mapping, and genomic structure of an X-linked gene for a subunit of human mitochondrial complex I.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human B22 subunit of the NADH-ubiquinone oxidoreductase maps to the region of chromosome 8 involved in branchio-oto-renal syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mitochondrial electron transport and oxidative phosphorylation system

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural organization and chromosomal localization of the human nuclear gene (NDUFV2) for the 24-kDa iron-sulfur subunit of complex I in mitochondrial respiratory chain

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the PSST subunit gene of human mitochondrial complex I to chromosome 19p13

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

cDNA sequence and chromosomal localization of the NDUFS8 human gene coding for the 23 kDa subunit of the mitochondrial complex I.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A human cDNA encoding the homologue of NADH: ubiquinone oxidoreductase subunit B13

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal localization of the human gene encoding the 51-kDa subunit of mitochondrial complex I (NDUFV1) to 11q13

1 reference

https://pubmed.ncbi.nlm.nih.gov/9686359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1005339332062

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9686359

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