(Q45373001)

English

Mitochondrial complex III deficiency caused by a homozygous UQCRC2 mutation presenting with neonatal-onset recurrent metabolic decompensation

scientific article published on 29 January 2013

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scholarly article

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Europe PubMed Central

13 December 2017

Mitochondrial complex III deficiency caused by a homozygous UQCRC2 mutation presenting with neonatal-onset recurrent metabolic decompensation (English)

1 reference

Europe PubMed Central

13 December 2017

1 reference

based on heuristic

inferred from title

Yoshinori Tsurusaki

12

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Europe PubMed Central

13 December 2017

Hirotomo Saitsu

object named as

Hirotomo Saitsu

15

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author name string

Noriko Miyake

1

1 reference

Europe PubMed Central

13 December 2017

Shoji Yano

2

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Europe PubMed Central

13 December 2017

Chika Sakai

3

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Europe PubMed Central

13 December 2017

Hideyuki Hatakeyama

4

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Europe PubMed Central

13 December 2017

Yuichi Matsushima

5

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Europe PubMed Central

13 December 2017

Masaaki Shiina

6

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Europe PubMed Central

13 December 2017

Yoriko Watanabe

7

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Europe PubMed Central

13 December 2017

James Bartley

8

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Europe PubMed Central

13 December 2017

Jose E Abdenur

9

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Europe PubMed Central

13 December 2017

Raymond Y Wang

10

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Europe PubMed Central

13 December 2017

Richard Chang

11

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Europe PubMed Central

13 December 2017

Hiroshi Doi

13

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Europe PubMed Central

13 December 2017

Mitsuko Nakashima

14

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Europe PubMed Central

13 December 2017

Kazuhiro Ogata

16

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Europe PubMed Central

13 December 2017

Yu-Ichi Goto

17

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Europe PubMed Central

13 December 2017

Naomichi Matsumoto

18

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Europe PubMed Central

13 December 2017

publication date

29 January 2013

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Europe PubMed Central

13 December 2017

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Europe PubMed Central

13 December 2017

34

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13 December 2017

3

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Europe PubMed Central

13 December 2017

446-452

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Europe PubMed Central

13 December 2017

Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Respiratory-chain diseases related to complex III deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Mitochondrial respiratory-chain diseases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Predicting changes in the stability of proteins and protein complexes: a study of more than 1000 mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Missense mutations in the BCS1L gene as a cause of the Björnstad syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Complete structure of the 11-subunit bovine mitochondrial cytochrome bc1 complex

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Performance of protein stability predictors.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Supercomplexes in the respiratory chains of yeast and mammalian mitochondria

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Rapid detection of a mutation causing X-linked leucoencephalopathy by exome sequencing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

Allegro version 2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

21 January 2018

A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22257

7 January 2021

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inferred from DOI database lookup

Identifiers

10.1002/HUMU.22257

1 reference

Europe PubMed Central

13 December 2017

1 reference

Europe PubMed Central

13 December 2017

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