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Late-onset Bartter syndrome type II
Mutations in the ROMK1 potassium channel gene (KCNJ1) cause antenatal/neonatal Bartter syndrome type II (aBS II), a renal disorder that begins in utero, accounting for the polyhydramnios and premature delivery that is typical in affected infants, who develop massive renal salt wasting, hypokalaemic...
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| Publicat a: | Clin Kidney J |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5622898/ https://ncbi.nlm.nih.gov/pubmed/28979772 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ckj/sfx033 |
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