SURFEIT-1 Gene Analysis and Two-Dimensional Blue Native Gel Electrophoresis in Cytochrome c Oxidase Deficiency-Reference-Cited by-同舟云学术

SURFEIT-1 Gene Analysis and Two-Dimensional Blue Native Gel Electrophoresis in Cytochrome c Oxidase Deficiency

Published:1999-11 Issue:2 Volume:265 Page:339-344
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Coenen Marieke J.H.,van den Heuvel Lambert P.,Nijtmans Leo G.J.,Morava Eva,Marquardt I.,Girschick Hermann J.,Trijbels Frans J.M.,Grivell Leslie A.,Smeitink Jan A.M.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference27 articles.

1. Getting to the Nucleus of Mitochondrial Disorders: Identification of Respiratory Chain–Enzyme Genes Causing Leigh Syndrome

2. Leigh syndrome: Clinical features and biochemical and DNA abnormalities

3. Cytochromec oxidase deficiency in leigh syndrome

4. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

5. The First Nuclear-Encoded Complex I Mutation in a Patient with Leigh Syndrome

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1. Causes of Death in Adults with Mitochondrial Disease;JIMD Reports;2015

2. The Heme a Synthase Cox15 Associates with Cytochrome c Oxidase Assembly Intermediates during Cox1 Maturation;Molecular and Cellular Biology;2013-10-15

3. Mitochondrial Cytochrome c Oxidase Assembly in Health and Human Diseases;Mitochondrial Disorders Caused by Nuclear Genes;2012-09-18

4. High-resolution melting analysis of 15 genes in 60 patients with cytochrome-c oxidase deficiency;Journal of Human Genetics;2012-05-17

5. SURF1-associated leigh syndrome: A case series and novel mutations;Human Mutation;2012-04-30