Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran.
| Autor: | Laleh, Masoud Akbarzadeh1, Naseri, Marzieh1, Poursadegh Zonouzi, Ali Akbar1, Poursadegh Zonouzi, Ahmad2, Masoudi, Marjan1, Ahangari, Najmeh1, Shams, Leila1, Nejatizadeh, Azim1 azimnejate@yahoo.com |
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| Zdroj: | Journal of Research in Medical Sciences. Aug2017, Vol. 22, p1-6. 6p. |
| Databáze: | Academic Search Ultimate |
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