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Autosomal recessive and sporadic deafness in Morocco: High frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant
Bouchaïb Gazzaz, Dominique Weil, Leïla Raïs, Omar Akhyat, Houssine Azeddoug, Sellama NadifiVolume:
210
Year:
2005
Language:
english
DOI:
10.1016/j.heares.2005.08.001
File:
PDF, 231 KB
english, 2005