A Large Consanguineous Family with a Mild and Transient form of Autosomal Recessive Pseudohypoaldosteronism type 1 (PHA1) Caused by a Novel Mutation in the SCNN1A Gene: Functional Studies — Alexandra Efthymiadou (2018) | RDL Network
A Large Consanguineous Family with a Mild and Transient form of Autosomal Recessive Pseudohypoaldosteronism type 1 (PHA1) Caused by a Novel Mutation in the SCNN1A Gene: Functional Studies
Alexandra Efthymiadou, Ivan Gautschi, Miguel X. van Bemmelen, Amalia Sertedaki, Aristeidis Giannakopoulos, George Chrousos, Laurent Schild, Dionisios Chrysis
Berenice B. Mendonça, Maristela V. Leite, Margaret de Castro, Tomoshige Kino, Lucila Leico Kagohara Elias, Tânia A.S.S. Bachega, Ivo J.P. Arnhold, George Chrousos, Ana Claudia Latrônico
Amalia Sertedaki, Tomoshige Kino, Christina Merakou, Dax A. Hoffman, Michael M. Hatch, Darrell E. Hurt, Lin Lin, Paraskevi Xekouki, Constantine A. Stratakis, George Chrousos, Evangelia Charmandari
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