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Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.

Bartter syndrome (BS) is a family of disorders manifested by hypokalemic hypochloremic metabolic alkalosis with normotensive hyperreninemic hyperaldosteronism. We evaluated a unique, inbred Bedouin kindred in which sensorineural deafness (SND) cosegregates with an infantile variant of the BS phenoty...

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Detalhes bibliográficos
Main Authors: Brennan, T M, Landau, D, Shalev, H, Lamb, F, Schutte, B C, Walder, R Y, Mark, A L, Carmi, R, Sheffield, V C
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1376884/
https://ncbi.nlm.nih.gov/pubmed/9463315
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