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Genetic etiology study of four Chinese families with two nonsyndromic deaf children in succession by targeted next‐generation sequencing
BACKGROUND: Genetic components contribute significantly to the cause of hearing loss. Nonsyndromic hearing loss has been shown to have high genetic heterogeneity. For families who had given birth to two nonsyndromic deaf children in succession, it seems that their deafness was highly related to gene...
Gorde:
| Argitaratua izan da: | Mol Genet Genomic Med |
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| Egile Nagusiak: | , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
John Wiley and Sons Inc.
2021
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8123758/ https://ncbi.nlm.nih.gov/pubmed/33638616 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1634 |
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