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Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82

Mendelian DisorderGenetic DisorderMedicineGeneticsWhole Exome SequencingMolecular BiologyMolecular GeneticsDisease Gene IdentificationGenomicsMolecular Diagnostics