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

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 | M. Koch | F. Hildebrandt | L. Guay-Woodford | M. Konrad | G. Deschênes | C. J. Wright | S. Hebert | N. Knoers | L. Monnens | P. Niaudet | W. Nillesen | L. Forestier | L. Heuvel | H. Seyberth | J. Alessandri | W. Proesmans | H. Lemmink | G. Madrigal | M. Brandis | D. Feldmann | D. K. Zimmermann | P. Saunier | C. Wieg | R. Vargas | B. Roth | M. Vollmer | G. Jean | M. Deschaux | E. Cougoureux | Frederique Lorridon | L. David | Arnold Kockerling | Karl-Heinz Grze chik | F. Laroze