Pages that link to "Q49915030"
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The following pages link to Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss (Q49915030):
Displaying 4 items.
- Small fish, big prospects: using zebrafish to unravel the mechanisms of hereditary hearing loss (Q89734622) (← links)
- Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines (Q91593468) (← links)
- An Immunological Perspective to Non-syndromic Sensorineural Hearing Loss (Q92538498) (← links)
- Gene therapy development in hearing research in China (Q97587562) (← links)