Sensorineural hearing loss in OPA1-linked disorders

The Mitochondrial Connection in Auditory Neuropathy

(2011) Anthony T. Cacace et al.   AUDIOLOGY AND NEURO-OTOLOGY

Auditory neuropathies

(2011) Fabrice Giraudet et al.   CURRENT OPINION IN NEUROLOGY

Auditory function in individuals within Leber’s hereditary optic neuropathy pedigrees

(2011) Gary Rance et al.   JOURNAL OF NEUROLOGY

Information from cochlear potentials and genetic mutations helps localize the lesion site in auditory neuropathy

(2011) Rosamaria Santarelli   Genome Medicine

Multi-system neurological disease is common in patients with OPA1 mutations

(2010) P. Yu-Wai-Man et al.   BRAIN

Vestibular dysfunction in a Japanese patient with a mutation in the gene OPA1

(2010) Kunio Mizutari et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals

(2009) Taosheng Huang et al.   BRAIN RESEARCH

Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novelOPA1mutations

(2009) Marc Ferré et al.   HUMAN MUTATION

OPA1-associated disorders: Phenotypes and pathophysiology

(2009) Patrizia Amati-Bonneau et al.   INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY

Hereditary optic neuropathies share a common mitochondrial coupling defect

(2008) Arnaud Chevrollier et al.   ANNALS OF NEUROLOGY

Progressive External Ophthalmoplegia and Vision and Hearing Loss in a Patient With Mutations in POLG2 and OPA1

(2008) Silvio Ferraris et al.   ARCHIVES OF NEUROLOGY

A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation

(2008) M. Liguori et al.   JOURNAL OF NEUROLOGY

OPA1 IN MULTIPLE MITOCHONDRIAL DNA DELETION DISORDERS

(2008) J. D. Stewart et al.   NEUROLOGY

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

(2007) P. Amati-Bonneau et al.   BRAIN