Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families-Reference-Cited by-同舟云学术

Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families

Published:2017-11 Issue: Volume:382 Page:29-35
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Pretegiani E.,Rosini F.,Rufa A.,Gallus G.N.,Cardaioli E.,Da Pozzo P.,Bianchi S.,Serchi V.,Collura M.,Franceschini R.,Bianchi Marzoli S.,Dotti M.T.,Federico A.

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference44 articles.

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4. Retinal nerve fiber layer thickness in dominant optic atrophy measurements by optical coherence tomography and correlation with age;Barboni;Ophthalmology,2011

5. Inherited mitochondrial optic neuropathies;Yu-Wai-Man;J. Med. Genet.,2009

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