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.