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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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Detalles Bibliográficos
Autores principales: Gollasch, Benjamin, Anistan, Yoland-Marie, Canaan-Kühl, Sima, Gollasch, Maik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622898/
https://www.ncbi.nlm.nih.gov/pubmed/28979772
http://dx.doi.org/10.1093/ckj/sfx033