Mutation Screening in Patients With Isolated Cytochrome c Oxidase Deficiency-Reference-Cited by-同舟云学术

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Mutation Screening in Patients With Isolated Cytochrome c Oxidase Deficiency

Published:2003-02 Issue:2 Volume:53 Page:224-230
ISSN:0031-3998
Container-title:Pediatric Research
language:en
Short-container-title:Pediatric Research

Author:

SACCONI SABRINA,SALVIATI LEONARDO,SUE CAROLYN M.,SHANSKE SARA,DAVIDSON MERCY M.,BONILLA EDUARDO,NAINI ALI B.,DE VIVO, AND DARRYL C.,DIMAURO SALVATORE

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference39 articles.

1. CYTOCHROME C OXIDASE: Structure and Spectroscopy

2. Cytochrome c oxidase deficiency

3. Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

4. A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency

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