Report on the p.Ser489X (p.Ser489*) CFTR mutation, a variant with severe associated phenotype and high prevalence in a Quebec French-Canadian cystic fibrosis patient population
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2015 ◽
Vol 50
(2)
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pp. 133-140
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2017 ◽
Vol 102
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pp. 133-137
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2021 ◽
Vol 40
(4)
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pp. S503-S504
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