Update 4/23/19 Added CEACAM16 to the Autosomal Recessive page Added GAB1 as the cause of… Added GAB1 as the cause of DFNB26 with METTL13 as DFNM1 modifier GRAP as a cause of ARNSHL Corrected links on the… 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 Syndromic hearing loss pages added 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 Current page 3
Added GAB1 as the cause of… Added GAB1 as the cause of DFNB26 with METTL13 as DFNM1 modifier 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
Update 4/23/19
Added CEACAM16 to the Autosomal Recessive page
Added GAB1 as the cause of…
Added
GAB1 as the cause of DFNB26 with METTL13 as DFNM1 modifier
GRAP as a cause of ARNSHL
Corrected links on the…
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
Syndromic hearing loss pages added
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