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. Update 9/20/18 The following genes were added: Dominant: DFNA7 LMX1A (Wesdorp et al., 2018)Dominant: PDE1C (Wang et al., 2018)Recessive: MPZL2 (Wesdorp et al., 2018)Dominant: REST (Nakano et al., 2018) Pagination First page « First Previous page ‹ Previous Page 1 Page 2 Page 3 Page 4
Update 1/17/19 Added GAB1 as the cause of DFNB26 with METTL13 as DFNM1 modifier.Added GRAP as a cause of ARNSHL.
Update 9/20/18 The following genes were added: Dominant: DFNA7 LMX1A (Wesdorp et al., 2018)Dominant: PDE1C (Wang et al., 2018)Recessive: MPZL2 (Wesdorp et al., 2018)Dominant: REST (Nakano et al., 2018)
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.
Update 9/20/18
The following genes were added:
Dominant: DFNA7 LMX1A (Wesdorp et al., 2018)
Dominant: PDE1C (Wang et al., 2018)
Recessive: MPZL2 (Wesdorp et al., 2018)
Dominant: REST (Nakano et al., 2018)