(Q60677988)

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Recurrence of the R947X Mutation in Unrelated Families with Autosomal Dominant Pseudohypoaldosteronism Type 1: Evidence for a Mutational Hot Spot in the Mineralocorticoid Receptor Gene

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  • Recurrence of the R947X mutation in unrelated families with autosomal dominant pseudohypoaldosteronism type 1: evidence for a mutational hot spot in the mineralocorticoid receptor gene
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Recurrence of the R947X Mutation in Unrelated Families with Autosomal Dominant Pseudohypoaldosteronism Type 1: Evidence for a Mutational Hot Spot in the Mineralocorticoid Receptor Gene (English)
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Recurrence of the R947X mutation in unrelated families with autosomal dominant pseudohypoaldosteronism type 1: evidence for a mutational hot spot in the mineralocorticoid receptor gene (English)
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Fabio L. Fernandes-Rosa
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Margaret de Castro
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Ana Claudia Latronico
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Wolfgang G. Sippell
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Felix G. Riepe
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Sonir R. Antonini
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Fabio L Fernandes-Rosa
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Wolfgang G Sippell
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Felix G Riepe
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Sonir R Antonini
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September 2006
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91
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9
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3671-3675
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3671-5
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