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Drosophila model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy

Autosomal dominant optic atrophy (DOA) is a progressive form of blindness caused by degeneration of retinal ganglion cells and their axons, mainly caused by mutations in the OPA1 mitochondrial dynamin like GTPase (OPA1) gene. OPA1 encodes a dynamin-like GTPase present in the mitochondrial inner memb...

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Principais autores: Yohei Nitta, Jiro Osaka, Ryuto Maki, Satoko Hakeda-Suzuki, Emiko Suzuki, Satoshi Ueki, Takashi Suzuki, Atsushi Sugie
Format: Artigo
Sprog:Inglês
Udgivet: eLife Sciences Publications Ltd 2024-08-01
Serier:eLife
Fag:
dominant optic atrophy
Drosophila
OPA1
axonal degeneration
Online adgang:https://elifesciences.org/articles/87880
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