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Αλέξανδρος Γ. Σφακιανάκης

Wednesday, November 18, 2020

Clinical heterogeneity of the SLC26A4 gene in UAE patients with hearing loss and bioinformatics investigation of DFNB4/Pendred syndrome missense mutations

xlomafota13 shared this article with you from Inoreader

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Publication date: Available online 9 November 2020

Source: International Journal of Pediatric Otorhinolaryngology

Author(s): Jihen Chouchen, Mona Mahfood, Maryam Alobathani, Walaa Kamal Eldin Mohamed, Abdelaziz Tlili

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