Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss

BACKGROUND: Hereditary hearing loss (HL) is a heterogeneous and most common sensory neural disorder. At least, 76 genes have been reported in association with autosomal recessive nonsyndromic HL (ARNSHL). Herein, we subjected two patients with bilateral sensorineural HL in two distinct consanguineou...

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Detalles Bibliográficos
Autores principales: Zardadi, Safoura, Razmara, Ehsan, Asgaritarghi, Golareh, Jafarinia, Ehsan, Bitarafan, Fatemeh, Rayat, Sima, Almadani, Navid, Morovvati, Saeid, Garshasbi, Masoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767568/
https://www.ncbi.nlm.nih.gov/pubmed/33205915
http://dx.doi.org/10.1002/mgg3.1550

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767568/
https://www.ncbi.nlm.nih.gov/pubmed/33205915
http://dx.doi.org/10.1002/mgg3.1550

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