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Distal Renal Tubular Acidosis in an Iranian Patient with Hereditary Spherocytosis
BACKGROUND: Hereditary spherocytosis and hereditary dRTA are associated with mutations in the SLC4A1 gene encoding the AE1. In this study, some patients with clinical evidence of congenital HS and renal symptoms were investigated. METHODS: Twelve patients with congenital HS and renal symptoms were r...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Pasteur Institute of Iran
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487683/ https://www.ncbi.nlm.nih.gov/pubmed/34481427 http://dx.doi.org/10.52547/ibj.25.5.359 |