Bartter Syndrome and GH Deficiency: three siblings with a novel CLCNKB mutation

Pediatrics International,Volume 0, Issue ja, -Not available-.

Source: Pediatrics International - November 2, 2018 Category: Pediatrics Authors: Ilaria Brambilla, Dimitri Poddighe, Simona Semeria Mantelli, Carmen Guarracino, Gian Luigi Marseglia Source Type: research