The first case of NSHL by direct impression on EYA1 gene and identification of one novel mutation in MYO7A in the Iranian families.
| Autor: | Razmara, Ehsan1, Bitarafan, Fatemeh2, Esmaeilzadeh-Gharehdaghi, Elika1, Almadani, Navid3, Garshasbi, Masoud1,2 masoud.garshasbi@modares.ac.ir |
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| Zdroj: | Iranian Journal of Basic Medical Sciences. Mar2018, Vol. 21 Issue 3, p333-341. 8p. |
| Databáze: | Academic Search Ultimate |
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