(Q39019353)
Statements
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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 (English)
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Sellama Nadifi
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Bouchaïb Gazzaz
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Dominique Weil
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Leïla Raïs
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Omar Akhyat
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Houssine Azeddoug
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21 October 2005
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210
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1-2
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80-84
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Identifiers
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