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)
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)