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Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families
The current molecular genetic diagnostic rates for hereditary hearing loss (HL) vary considerably according to the population background. Pakistan and other countries with high rates of consanguineous marriages have served as a unique resource for studying rare and novel forms of recessive HL. A com...
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| Vydáno v: | Genes (Basel) |
|---|---|
| Hlavní autoři: | , , , , , , , , , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7709052/ https://ncbi.nlm.nih.gov/pubmed/33187236 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11111329 |
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