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Journal Articles Revue Méditerranéenne de Génétique Humaine Year : 2010

La mucoviscidose au Maroc, mais où sont passés les malades?

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Abstract

Cystic fibrosis (CF) is a severe autosomal recessive disease most common in Caucasian populations. It is characterized by a great clinical variability. Over 1500 mutations have been described in the CFTR gene www.genet.sickkids.on.ca / CFTR, with geographical and ethnic variations in the distribution and frequency of mutations. The clinical and mutational profiles of CF of the native Moroccan population are unknown. The only existing studies concern patients of Moroccan origin living in Europe and Israel. We discuss the results of a recent work in which we estimated that the prevalence of CF in the native Moroccan population between 1 / 1680 and 1 / 4150.
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hal-00634746 , version 1 (23-10-2011)

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  • HAL Id : hal-00634746 , version 1

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Ilham Ratbi, Abdelaziz Sefiani. La mucoviscidose au Maroc, mais où sont passés les malades?. Revue Méditerranéenne de Génétique Humaine, 2010, 1, pp.45-46. ⟨hal-00634746⟩

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