(Q45356787)
Statements
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Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1. (English)
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Maik Welzel
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Leyla Akin
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Anja Büscher
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Tülay Güran
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Berthold P Hauffa
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Wolfgang Högler
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Julia Leonards
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Beate Karges
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Heiner Kentrup
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Birgul Kirel
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Emine Esin Yalinbas Senses
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Neslihan Tekin
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Paul-Martin Holterhus
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Felix G Riepe
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15 April 2013
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Identifiers
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