Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden

Mutations in connexins are the most common causes of hearing impairment (HI) in many populations. Our aim was to review the global burden of pathogenic and likely pathogenic (PLP) variants in connexin genes associated with HI. We conducted a systematic review of the literature based on targeted incl...

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Detalles Bibliográficos
Autores principales: Adadey, Samuel Mawuli, Wonkam-Tingang, Edmond, Twumasi Aboagye, Elvis, Nayo-Gyan, Daniel Wonder, Boatemaa Ansong, Maame, Quaye, Osbourne, Awandare, Gordon A., Wonkam, Ambroise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693846/
https://www.ncbi.nlm.nih.gov/pubmed/33126609
http://dx.doi.org/10.3390/life10110258

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693846/
https://www.ncbi.nlm.nih.gov/pubmed/33126609
http://dx.doi.org/10.3390/life10110258

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