CONNEXIN 26 MUTATIONS ASSOCIATED WITH THE MOST COMMON FORM OF NON SYNDROMIC NEUROSENSORY AUTOSOMAL RECESSIVE DEAFNESS (DFNB1) IN MEDITERRANEANS

ZELANTE, L., GASPARINI, P., ESTIVILL, X., MELCHIONDA, S., D AGRUMA, L., GOVEA, N., & MILA, M.. (1997). CONNEXIN 26 MUTATIONS ASSOCIATED WITH THE MOST COMMON FORM OF NON SYNDROMIC NEUROSENSORY AUTOSOMAL RECESSIVE DEAFNESS (DFNB1) IN MEDITERRANEANS. HUMAN MOLECULAR GENETICS, 6(9), 1605-1609. SID. https://sid.ir/paper/550667/en

ZELANTE L., GASPARINI P., ESTIVILL X., MELCHIONDA S., D AGRUMA L., GOVEA N., MILA M.. CONNEXIN 26 MUTATIONS ASSOCIATED WITH THE MOST COMMON FORM OF NON SYNDROMIC NEUROSENSORY AUTOSOMAL RECESSIVE DEAFNESS (DFNB1) IN MEDITERRANEANS. HUMAN MOLECULAR GENETICS[Internet]. 1997;6(9):1605-1609. Available from: https://sid.ir/paper/550667/en

L. ZELANTE, P. GASPARINI, X. ESTIVILL, S. MELCHIONDA, L. D AGRUMA, N. GOVEA, and M. MILA, “CONNEXIN 26 MUTATIONS ASSOCIATED WITH THE MOST COMMON FORM OF NON SYNDROMIC NEUROSENSORY AUTOSOMAL RECESSIVE DEAFNESS (DFNB1) IN MEDITERRANEANS,” HUMAN MOLECULAR GENETICS, vol. 6, no. 9, pp. 1605–1609, 1997, [Online]. Available: https://sid.ir/paper/550667/en