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

Genome Medicine

Volumn 2, Issue 12, 2011, Pages

  Santarelli, Rosamaria ^a  

^a UNIVERSITY OF PADOVA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ATAXIA; AUDITORY STIMULATION; AUDITORY THRESHOLD; BRAIN STEM; CARDIOMYOPATHY; CELL ACTIVITY; COCHLEA POTENTIAL; COCHLEA PROSTHESIS; COCHLEAR NERVE; CONGENITAL DEAFNESS; DEMENTIA; DEMYELINATING NEUROPATHY; DOMINANT INHERITANCE; DYSTONIA; ELECTROCOCHLEOGRAPHY; ELECTROSTIMULATION; GENE LOCUS; GENE MUTATION; GIANT AXONAL NEUROPATHY; HAIR CELL; HEARING LOSS; HUMAN; MISSENSE MUTATION; MITOCHONDRIAL GENE; MOLECULAR MECHANICS; NERVE CONDUCTION; NERVE ENDING; OPTIC NERVE ATROPHY; OPTIC NERVE DISEASE; PERIPHERAL NEUROPATHY; PRESYNAPTIC NERVE; PRIORITY JOURNAL; RECESSIVE INHERITANCE; REVIEW; SPEECH PERCEPTION; SYNAPSE; VESTIBULOCOCHLEAR NERVE DISEASE;

EID: 78751689056     PISSN: None     EISSN: 1756994X     Source Type: Journal    
DOI: 10.1186/gm212     Document Type: Review

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