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1. Bartter syndrome and growth hormone deficiency: Three siblings with a novel CLCNKB mutation.

Author

Brambilla I, Poddighe D, Semeria Mantelli S, Guarracino C, and Marseglia GL

Subjects
Bartter Syndrome complications, Child, Child, Preschool, Diagnosis, Differential, Dwarfism, Pituitary complications, Dwarfism, Pituitary diagnosis, Female, Genetic Testing methods, Growth Hormone therapeutic use, Humans, Male, Mutation, Potassium blood, Siblings, Bartter Syndrome genetics, Chloride Channels genetics, Dwarfism, Pituitary genetics, Growth Hormone blood
Published
2019
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