Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder

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Predicting the Functional Effect of Amino Acid Substitutions and Indels

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

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Severe X-Linked Mitochondrial Encephalomyopathy Associated with a Mutation in Apoptosis-Inducing Factor

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The genetic basis of auditory neuropathy spectrum disorder (ANSD)

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Imaging Characteristics of Children With Auditory Neuropathy Spectrum Disorder

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Life with or without AIF

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Evaluation of inner hair cell and nerve fiber loss as sufficient pathologies underlying auditory neuropathy

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Prevalence of auditory neuropathy (AN) among infants and young children with severe to profound hearing loss

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Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

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Auditory neuropathy: Endocochlear lesion or temporal processing impairment? Implications for diagnosis and management

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