Bartter syndrome and growth hormone deficiency

Three siblings with a novel CLCNKB mutation

Ilaria Brambilla, Dimitri Poddighe, Simona Semeria Mantelli, Carmen Guarracino, Gian Luigi Marseglia

Research output: Contribution to journalComment/debate

Original languageEnglish
Pages (from-to)193-197
Number of pages5
JournalPediatrics International
Volume61
Issue number2
DOIs
Publication statusPublished - Feb 1 2019

Fingerprint

Bartter Syndrome
Failure to Thrive
Growth Hormone
Mutation

Keywords

  • Bartter syndrome
  • CLCNKB
  • failure to thrive
  • growth hormone deficiency

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Bartter syndrome and growth hormone deficiency : Three siblings with a novel CLCNKB mutation. / Brambilla, Ilaria; Poddighe, Dimitri; Semeria Mantelli, Simona; Guarracino, Carmen; Marseglia, Gian Luigi.

In: Pediatrics International, Vol. 61, No. 2, 01.02.2019, p. 193-197.

Research output: Contribution to journalComment/debate

Brambilla, Ilaria ; Poddighe, Dimitri ; Semeria Mantelli, Simona ; Guarracino, Carmen ; Marseglia, Gian Luigi. / Bartter syndrome and growth hormone deficiency : Three siblings with a novel CLCNKB mutation. In: Pediatrics International. 2019 ; Vol. 61, No. 2. pp. 193-197.
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