OPA1 functions in mitochondria and dysfunctions in optic nerve-Reference-Cited by-同舟云学术

OPA1 functions in mitochondria and dysfunctions in optic nerve

Published:2009-10 Issue:10 Volume:41 Page:1866-1874
ISSN:1357-2725
Container-title:The International Journal of Biochemistry & Cell Biology
language:en
Short-container-title:The International Journal of Biochemistry & Cell Biology

Author:

Lenaers Guy,Reynier Pascal,ElAchouri Ghizlane,Soukkarieh Chadi,Olichon Aurélien,Belenguer Pascale,Baricault Laurent,Ducommun Bernard,Hamel Christian,Delettre Cécile

Publisher

Elsevier BV

Subject

Cell Biology,Biochemistry

Reference93 articles.

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3. Characterization of OPA1 isoforms isolated from mouse tissues;Akepati;J Neurochem,2008

4. A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy;Alavi;Brain,2007

5. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28;Alexander;Nat Genet,2000

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