Frederique Lorridon

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes.

A. Ziegler, K. Grzeschik, G. Rizzoni, 1997, Human molecular genetics.

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity

A. Ziegler, G. Rizzoni, C. Antignac, 2019 .