Rare Gene Mutations in Romanian Hypoacusis Patients: Case Series and a Review of the Literature

(1) Background: In this paper, we report on three cases of hypoacusis as part of a complex phenotype and some rare gene variants. An extensive review of literature completes the newly reported clinical and genetic information. (2) Methods: The cases range from 2- to 11-year-old boys, all with a comp...

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Detalhes bibliográficos

Principais autores:	Alexandra-Cristina Neagu, Magdalena Budișteanu, Dan-Cristian Gheorghe, Adela-Ioana Mocanu, Horia Mocanu
Formato:	Artigo
Idioma:	Inglês
Publicado em:	MDPI AG 2022-09-01
coleção:	Medicina
Assuntos:	genetics of hearing loss mutations rare hypoacusis mitochondrial TWNK
Acesso em linha:	https://www.mdpi.com/1648-9144/58/9/1252
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