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Gradual Symmetric Progression of DFNA34 Hearing Loss Caused by an NLRP3 Mutation and Cochlear Autoinflammation
OBJECTIVE: To characterize the audiometric phenotype of autosomal dominant DFNA34 hearing loss (HL) caused by a missense substitution in the NLRP3 gene. NLRP3 encodes a critical component of the NLRP3 inflammasome that is activated in innate immune responses. STUDY DESIGN: This study was conducted u...
Tallennettuna:
| Julkaisussa: | Otol Neurotol |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5807171/ https://ncbi.nlm.nih.gov/pubmed/29342053 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MAO.0000000000001715 |
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