A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family
Bewaard in:
| Hoofdauteurs: | , , , , , , , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Wolters Kluwer
2022-11-01
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| Reeks: | Chinese Medical Journal |
| Online toegang: | http://journals.lww.com/10.1097/CM9.0000000000001966 |
| Tags: |
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