Pax3 deficiency diminishes melanocytes in the developing mouse cochlea

Cochlear melanocytes are intermediate cells in the stria vascularis that generate endocochlear potentials required for auditory function. Human PAX3 mutations cause Waardenburg syndrome and abnormalities of melanocytes, manifested as congenital hearing loss and hypopigmentation of skin, hair and eye...

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Detalles Bibliográficos
Autores principales: Udagawa, Tomokatsu, Takahashi, Erisa, Tatsumi, Norifumi, Mutai, Hideki, Kondo, Yuko, Atkinson, Patrick J., Matsunaga, Tatsuo, Yoshikawa, Mamoru, Kojima, Hiromi, Okabe, Masataka, Cheng, Alan G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274955/
https://www.ncbi.nlm.nih.gov/pubmed/37333245
http://dx.doi.org/10.21203/rs.3.rs-2990436/v1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274955/
https://www.ncbi.nlm.nih.gov/pubmed/37333245
http://dx.doi.org/10.21203/rs.3.rs-2990436/v1

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