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Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy

✍ Scribed by Sharareh Dadgar; Olivier Hagens; Seyed Razi Dadgar; Ehsan Nobakht Haghighi; Simone Schimpf; Bernd Wissinger; Masoud Garshasbi

Book ID: 116456447
Publisher: Elsevier Science
Year: 2006
Tongue: English
Weight: 381 KB
Volume: 83
Category: Article
ISSN: 0014-4835
DOI: 10.1016/j.exer.2006.03.004

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