SCD5 Added SCD5 (Lu et al., 2020) to ADNSHL page. PLS1 Added PLS1 (Morgan et al., 2019) to ADNSHL page. TRRAP Added TRRAP (Xia et al., 2019) to ADNSHL page. CLDN9 Added CLDN9 to ARNSHL page. SPNS2 Added SPNS2 to ARNSHL page. Update 4/23/19 Added CEACAM16 to ARNSHL page. Update 1/17/19 Added GAB1 as the cause of DFNB26 with METTL13 as DFNM1 modifier.Added GRAP as a cause of ARNSHL. Update 1/8/19 Corrected links on the autosomal recessive and X-linked pages. Update 9/30/18 Dominant: DFNA37 COL11A1 (Booth et al., 2018) Update 9/27/18 Added syndromic hearing loss pages. Pagination First page « First Previous page ‹ Previous Page 1 Page 2 Page 3 Page 4 Page 5 Next page Next › Last page Last »
Update 1/17/19 Added GAB1 as the cause of DFNB26 with METTL13 as DFNM1 modifier.Added GRAP as a cause of ARNSHL.
SCD5
Added SCD5 (Lu et al., 2020) to ADNSHL page.
PLS1
Added PLS1 (Morgan et al., 2019) to ADNSHL page.
TRRAP
Added TRRAP (Xia et al., 2019) to ADNSHL page.
CLDN9
Added CLDN9 to ARNSHL page.
SPNS2
Added SPNS2 to ARNSHL page.
Update 4/23/19
Added CEACAM16 to ARNSHL page.
Update 1/17/19
Update 1/8/19
Corrected links on the autosomal recessive and X-linked pages.
Update 9/30/18
Dominant: DFNA37 COL11A1 (Booth et al., 2018)
Update 9/27/18
Added syndromic hearing loss pages.