Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Pseudohypoaldosteronism and SCNN1A[original query] |
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Association of a sodium channel alpha subunit promoter variant with blood pressure. Journal of the American Society of Nephrology : JASN 2002 Jan 13 (1): 80-5. Iwai Naoharu, Baba Shunroku, Mannami Toshifumi, Ogihara Toshio, Ogata J |
A Novel SCNN1A Variation in a Patient with Autosomal-recessive Pseudohypoaldosteronism Type 1. Journal of clinical research in pediatric endocrinology 2021 4 14 (2): 244-250. Huneif Mohammed Ayed, Alhazmy Ziyad Hamad, Shoomi Anas M., Alghofely Mohammed A., Heena Humariya, Mushiba Aziza M., AlSaheel Abdulham |
A mild and transient form of autosomal recessive Pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation in the SCNN1A gene. American journal of physiology. Endocrinology and metabolism 2023 5 . Alexandra Eythymiadou, Ivan Gautschi, Miguel Xavier van Bemmelen, Amalia Sertedaki, Aristeidis Giannakopoulos, George Chrousos, Laurent Schild, Dionisios Chrys |
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