Machine Learning to Identify Genetic Salt-Losing Tubulopathies in Hypokalemic Patients

INTRODUCTION: Clinically distinguishing patients with the inherited salt-losing tubulopathies (SLTs), Gitelman or Bartter syndrome (GS or BS) from other causes of hypokalemia (LK) patients is difficult, and genotyping is costly. We decided to identify clinical characteristics that differentiate SLTs...

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Detalles Bibliográficos
Autores principales: Wan, Elizabeth R., Iancu, Daniela, Ashton, Emma, Siew, Keith, Mohidin, Barian, Sung, Chih-Chien, Nagano, China, Bockenhauer, Detlef, Lin, Shih-Hua, Nozu, Kandai, Walsh, Stephen B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014379/
https://www.ncbi.nlm.nih.gov/pubmed/36938092
http://dx.doi.org/10.1016/j.ekir.2022.12.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014379/
https://www.ncbi.nlm.nih.gov/pubmed/36938092
http://dx.doi.org/10.1016/j.ekir.2022.12.008

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