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Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technology
BACKGROUND: Recent advances in molecular genetics have enabled to determine the genetic causes of non-syndromic hearing loss, and more than 100 genes have been related to the phenotype. Due to this extraordinary genetic heterogeneity, a large percentage of patients remain without any molecular diagn...
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| Publicado no: | BMC Med Genet |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4581412/ https://ncbi.nlm.nih.gov/pubmed/26399936 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-015-0232-8 |
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