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A case report of apparent mineralocorticoid excess, with nephrological and neurological symptoms since birth, and with a new probably pathogenic variant in HSD11B2 gene
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Published in: | Nefrología 2024-11, Vol.44 (6), p.904-906 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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ISSN: | 2013-2514 2013-2514 |
DOI: | 10.1016/j.nefroe.2024.11.025 |