Usher Syndrome Belongs to the Genetic Diseases Associated with Radiosensitivity: Influence of the ATM Protein Kinase

Usher syndrome (USH) is a rare autosomal recessive disease characterized by the combination of hearing loss, visual impairment due to retinitis pigmentosa, and in some cases vestibular dysfunctions. Studies published in the 1980s reported that USH is associated with cellular radiosensitivity. Howeve...

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Detalles Bibliográficos
Autores principales: Al-Choboq, Joëlle, Ferlazzo, Mélanie L., Sonzogni, Laurène, Granzotto, Adeline, El-Nachef, Laura, Maalouf, Mira, Berthel, Elise, Foray, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836140/
https://www.ncbi.nlm.nih.gov/pubmed/35163494
http://dx.doi.org/10.3390/ijms23031570

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836140/
https://www.ncbi.nlm.nih.gov/pubmed/35163494
http://dx.doi.org/10.3390/ijms23031570

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