The Autosomal Dominant Syndrome of Progressive Optic Atrophy and Congenital Deafness

Author:

Kollarits Carol R.,Pinheiro Marilyn L.,Swann Edwin R.,Marcus Daniel F.,Corrie W. Stephen

Publisher

Elsevier BV

Subject

Ophthalmology

Reference8 articles.

1. Dominant congenital deafness and progressive optic atrophy;Konigsmark;Arch. Ophthalmol.,1974

2. Language development in the deaf child. A psycholinguistic approach;Fry,1977

3. Hearing in Children;Northern,1974

4. Genetic and metabolic deafness;Konigsmark,1976

5. The association of juvenile diabetes mellitus and optic atrophy. Clinical and genetic aspects;Rose;Q. J. Med.,1966

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1. Visual Loss;Liu, Volpe, and Galetta's Neuro-Ophthalmology;2019

2. A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16;Human Molecular Genetics;2011-02-24

3. Visual loss;Neuro-Ophthalmology;2010

4. Optic Nerve;Ocular Pathology;2009

5. Progressive autosomal dominant optic atrophy and sensorineural hearing loss in a Turkish family;Ophthalmic Genetics;2002-01

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