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First submitted to a journal in 1989, the article was finally published in 1992

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Hence, the predominant phenotypes described with AIFM1 mutations are either mitochondrial encephalomyopathies or sensorineural hearing loss and auditory neuropathy as transmission from the inner ear to the auditory nerve and brain stem is distorted [160]

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Imaging (CT with contrast or abdominal ultrasound) becomes interpretable