Gao et al., 2018
- Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss..
Journal of Medical Genetics
55(5):298-306
Full text @ J. Med. Genet.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | crfb4 | cytokine receptor family member b4 |
| Gene | ifnlr1 | interferon lambda receptor 1 |
| Gene | irf9 | interferon regulatory factor 9 |
| Gene | jak1 | Janus kinase 1 |
| Gene | lyz | lysozyme |
| Gene | stat1a | signal transducer and activator of transcription 1a |
| Gene | stat2 | signal transducer and activator of transcription 2 |
| Gene | stat3 | signal transducer and activator of transcription 3 (acute-phase response factor) |
| Gene | stat4 | signal transducer and activator of transcription 4 |
| Gene | stat5b | signal transducer and activator of transcription 5b |
| Gene | tyk2 | tyrosine kinase 2 |