A case of Ohtahara syndrome with cytochrome oxidase deficiency-Reference-Cited by-同舟云学术

A case of Ohtahara syndrome with cytochrome oxidase deficiency

Published:2008-11-12 Issue:8 Volume:40 Page:568-570
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:

Author:

Williams AN,Gray RG,MPhil K Poulton,MRCPath P Ramani,Whitehouse W P A

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1998.tb15416.x/fullpdf

Reference7 articles.

1. Structure and function of cytochrome C oxidase;Capaldi;Annual Review of Biochemistry,1995

2. Early infantile encephalopathy with suppression-burst: Ohtahara syndrome;Clarke;Developmental Medicine and Child Neurology,1987

3. On the specific age-dependent epileptic syndrome. The early-infantile epileptic encephalopathy with suppression burst;Ohtahara;No-To-Hattatsu (Tokyo),1976

4. Amicrodeletion in cytochrome C oxidase (COX) subunit III associated with COX deficiency and myoglobinuria;Keightley;Nature Genetics,1996

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