טוען...
Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort
BACKGROUND: Hearing loss or hearing impairment is a clinically and genetically heterogeneous disorder. More than 117 genes were discovered to date in hereditary, nonsyndromic hearing loss (NSHL). Identifying novel gene variants and their frequency in specific populations is valuable for public healt...
שמור ב:
| הוצא לאור ב: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
John Wiley and Sons Inc.
2019
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6732339/ https://ncbi.nlm.nih.gov/pubmed/31389194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.917 |
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