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Auditory dysfunction in type 2 Stickler Syndrome
PURPOSE: To present the extent and site of lesion of auditory dysfunction in a large cohort of individuals with type 2 Stickler Syndrome. Type 2 Stickler Syndrome results from a mutation in the gene coding for α-1 type XI pro-collagen, which has been identified in the human vitreous, cartilage and t...
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| 發表在: | Eur Arch Otorhinolaryngol |
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| Main Authors: | , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Springer Berlin Heidelberg
2020
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8165062/ https://ncbi.nlm.nih.gov/pubmed/32901364 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00405-020-06306-y |
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