HLA typing in Bartter syndrome

V. Delaney, A. J. Watson, M. Pollack, B. Dupont, E. Bourke

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

The mode of inheritance of Bartter syndrome is unclear; however, autosomal recessive inheritance seems likely. A consistent genetic marker of the carrier state likewise remains elusive. HLA typing was done in a family in whom six of 12 sibs have the syndrome. No significant HLA-syndrome linkage was found. This is in contrast to another familial hypokalemic syndrome in which a significant HLA association was found.

Original languageEnglish
Pages (from-to)779-782
Number of pages4
JournalAmerican Journal of Medical Genetics
Volume19
Issue number4
DOIs
StatePublished - 1984
Externally publishedYes

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