Alberto Bettinelli
Department of Pediatrics
San Leopoldo Mandic Hospital
Merate
and Department of Pediatrics and Neonatology
Italy
Name/email consistency: high
- Simultaneous mutations in the CLCNKB and SLC12A3 genes in two siblings with phenotypic heterogeneity in classic Bartter syndrome. Bettinelli, A., Borsa, N., Syrén, M.L., Mattiello, C., Coviello, D., Edefonti, A., Giani, M., Travi, M., Tedeschi, S. Pediatr. Res. (2005)