A novel frameshift variant in the TMPRSS3 gene causes nonsyndromic hearing loss in a consanguineous family.
| Autor: | Rezaie, Nahid1,2 (AUTHOR), Ghazanfari, Saeedeh Sadat3 (AUTHOR), Mousavikia, Seyede Mahsa4 (AUTHOR), Mansour Samaei, Nader1,5,6 (AUTHOR) n_samaei@yahoo.com, Oladnabi, Morteza1,5 (AUTHOR) oladnabidozin@yahoo.com, Sarli, Abdolazim4 (AUTHOR), Khosravi, Teymoor1 (AUTHOR) |
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| Zdroj: | BMC Medical Genomics. 11/29/2024, Vol. 17 Issue 1, p1-12. 12p. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
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