Загрузка...
Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss
BACKGROUND: Hereditary hearing loss (HL) is a heterogeneous and most common sensory neural disorder. At least, 76 genes have been reported in association with autosomal recessive nonsyndromic HL (ARNSHL). Herein, we subjected two patients with bilateral sensorineural HL in two distinct consanguineou...
Сохранить в:
| Опубликовано в: : | Mol Genet Genomic Med |
|---|---|
| Главные авторы: | , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
John Wiley and Sons Inc.
2020
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7767568/ https://ncbi.nlm.nih.gov/pubmed/33205915 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1550 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|