A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana.

Autor: Adadey, Samuel Mawuli1,2 (AUTHOR), Aboagye, Elvis Twumasi1,2 (AUTHOR), Esoh, Kevin2 (AUTHOR), Acharya, Anushree3 (AUTHOR), Bharadwaj, Thashi3 (AUTHOR), Lin, Nicole S.3 (AUTHOR), Amenga-Etego, Lucas1 (AUTHOR), Awandare, Gordon A.1 (AUTHOR), Schrauwen, Isabelle3 (AUTHOR), Leal, Suzanne M.3,4 (AUTHOR), Wonkam, Ambroise2,5 (AUTHOR) ambroise.wonkam@uct.ac.za
Zdroj: BMC Medical Genomics. 11/10/2022, Vol. 15 Issue 1, p1-10. 10p.
Databáze: Academic Search Ultimate
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