In silico and in vivo analyses of a novel variant in MYO 6 identified in a family with postlingual non-syndromic hearing loss from Argentina

Hereditary hearing loss stands as the most prevalent sensory disorder, with over 124 non-syndromic genes and approximately 400 syndromic forms of deafness identified in humans. The clinical presentation of these conditions spans a spectrum, ranging from mild to profound hearing loss. The aim of this...

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Veröffentlicht in:	NAR genomics and bioinformatics 2024-12, Vol.6 (4), p.lqae162
Hauptverfasser:	Buonfiglio, Paula I, Bruque, Carlos D, Salatino, Lucía, Lotersztein, Vanesa, Pace, Mariela, Grinberg, Sofia, Elgoyhen, Ana B, Plazas, Paola V, Dalamón, Viviana
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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