Condition: DEAFNESS, AUTOSOMAL RECESSIVE 68


rs869312749 in DNMT1;S1PR2 gene and DEAFNESS, AUTOSOMAL RECESSIVE 68 PMID 26805784 2016 Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2.

rs869312750 in S1PR2;DNMT1 gene and DEAFNESS, AUTOSOMAL RECESSIVE 68 PMID 26805784 2016 Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2.