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Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees
BACKGROUND: Clinical genetic diagnosis of non-syndromic hearing loss (NSHL) is quite challenging. With regard to its high heterogeneity as well as large size of some genes, it is also really difficult to detect causative mutations using traditional approaches. One of the recent technologies called w...
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| Vydáno v: | BMC Med Genet |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7672957/ https://ncbi.nlm.nih.gov/pubmed/33208113 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01168-x |
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