Condition: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)


rs879255246 in OTOF gene and DEAFNESS, AUTOSOMAL RECESSIVE (disorder) PMID 27082237 2016 Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia).