Bilateral persistent fetal vasculature and a chromosome 10 mutation including COX15-Reference-Cited by-同舟云学术

Bilateral persistent fetal vasculature and a chromosome 10 mutation including COX15

Published:2017-12 Issue:6 Volume:52 Page:e203-e205
ISSN:0008-4182
Container-title:Canadian Journal of Ophthalmology
language:en
Short-container-title:Canadian Journal of Ophthalmology

Author:

Hasbrook Madeleine,Yonekawa Yoshihiro,Van Laere Lily,Shah Ankoor R.,Capone Antonio

Publisher

Elsevier BV

Subject

Ophthalmology,General Medicine

Reference11 articles.

1. Early vitrectomy effective for bilateral combined anterior and posterior persistent fetal vasculature syndrome;Walsh;Retina,2010

2. Bilateral persistent fetal vasculature: a study of 11 cases;Kumar;J AAPOS,2010

3. Online Mendelian Inheritance in Man. Cytochrome c oxidase assembly protein COX15; COX15. Available at 〈www.omim.org/entry/603646〉. Accessed Feb. 13, 2016.

4. Isoforms of mammalian cytochrome c oxidase: correlation with human cytochrome c oxidase deficiency;Kennaway;Pediatr Res,1990

5. Functional and genetic studies demonstrate that mutation in the COX15 gene can cause Leigh syndrome;Oquendo;J Med Genet,2004

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