Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss (Q49915030)
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scientific article published on 16 February 2018
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss |
scientific article published on 16 February 2018 |
Statements
Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss (English)
1 reference
Xue Gao
1 reference
Yong-Yi Yuan
1 reference
Qiong-Fen Lin
1 reference
Jin-Cao Xu
1 reference
Wei-Qian Wang
1 reference
Yue-Hua Qiao
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Dong-Yang Kang
1 reference
Dan Bai
1 reference
Feng Xin
1 reference
Sha-Sha Huang
1 reference
Shi-Wei Qiu
1 reference
Li-Ping Guan
1 reference
Yu Su
1 reference
Guo-Jian Wang
1 reference
Ming-Yu Han
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Yi Jiang
1 reference
Han-Kui Liu
1 reference
Pu Dai
1 reference
16 February 2018
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55
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5
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298-306
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Identifiers
1 reference