OPA1 R445H mutation in optic atrophy associated with sensorineural deafness-Reference-Cited by-同舟云学术

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness

Published:2005 Issue:6 Volume:58 Page:958-963
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Amati-Bonneau Patrizia,Guichet Agnès,Olichon Aurélien,Chevrollier Arnaud,Viala Frédérique,Miot Stéphanie,Ayuso Carmen,Odent Sylvie,Arrouet Catherine,Verny Christophe,Calmels Marie-Noelle,Simard Gilles,Belenguer Pascale,Wang Jing,Puel Jean-Luc,Hamel Christian,Malthièry Yves,Bonneau Dominique,Lenaers Guy,Reynier Pascal

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference20 articles.

1. Dominant Congenital Deafness and Progressive Optic Nerve Atrophy

2. Progressive autosomal dominant optic atrophy and sensorineural hearing loss in a Turkish family

3. Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

4. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

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