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A2ML1 and otitis media: novel variants, differential expression and relevant pathways
A genetic basis for otitis media is established, however the role of rare variants in disease etiology is largely unknown. Previously a duplication variant within A2ML1 was identified as a significant risk factor for otitis media in an indigenous Filipino population and in US children. In this repor...
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| Опубликовано в: : | Hum Mutat |
|---|---|
| Главные авторы: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2019
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6711784/ https://ncbi.nlm.nih.gov/pubmed/31009165 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.23769 |
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