DeafnessHearing Loss, SensorineuralHearing LossCochleaPedigreeGenes, RecessiveEar, InnerEvoked Potentials, Auditory, Brain StemConnexinsSyndromeHearing Loss, UnilateralHair Cells, AuditoryStria VascularisSpiral GanglionHearingAudiometryCochlear ImplantsHearing Loss, BilateralDisabled PersonsConsanguinityCochlear ImplantationUsher SyndromesMutationLipreadingHearing TestsHearing Loss, CentralEndolymphSign LanguageWolfram SyndromeAuditory ThresholdWaardenburg SyndromeCochlear NerveAudiometry, Pure-ToneHypoparathyroidismOrgan of CortiHair Cells, Auditory, InnerCochlear DiseasesJervell-Lange Nielsen SyndromeGenetic LinkageStereociliaVestibular DiseasesTectorial MembraneDNA Mutational AnalysisPersons With Hearing ImpairmentsStapesHearing DisordersMutation, MissenseChromosome MappingTranscription Factor Brn-3CGenes, DominantPhenotypeHair ColorKCNQ Potassium ChannelsVestibular AqueductHearing Loss, ConductiveAbnormalities, MultipleLabyrinth DiseasesAtaxiaIchthyosisUnited StatesTemporal BoneCochlear DuctGoiterHair Cells, Auditory, OuterHearing AidsHomeless PersonsDNA, MitochondrialGenetic TestingVestibule, LabyrinthNephritis, HereditaryBulbar Palsy, ProgressiveIntellectual DisabilityAcoustic StimulationEarColobomaHomozygoteMolecular Sequence DataMentally Ill PersonsAuditory CortexPoint MutationRisk FactorsLod ScoreAuditory PerceptionNational Institute on Deafness and Other Communication Disorders (U.S.)Keratoderma, PalmoplantarPakistanHeterozygoteCochlear Nucleus