Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment

The genetic etiology of non-syndromic hearing impairment (NSHI) is highly heterogeneous with over 124 distinct genes identified. The wide spectrum of implicated genes has challenged the implementation of molecular diagnosis with equal clinical validity in all settings. Differential frequencies of al...

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Detalles Bibliográficos
Autores principales: Aboagye, Elvis Twumasi, Adadey, Samuel Mawuli, Wonkam-Tingang, Edmond, Amenga-Etego, Lucas, Awandare, Gordon A., Wonkam, Ambroise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Systematic Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9957346/
https://www.ncbi.nlm.nih.gov/pubmed/36833326
http://dx.doi.org/10.3390/genes14020399

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9957346/
https://www.ncbi.nlm.nih.gov/pubmed/36833326
http://dx.doi.org/10.3390/genes14020399

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