Cinacalcet Treatment in an Adolescent With Concurrent 22q11.2 Deletion Syndrome and Familial Hypocalciuric Hypercalcemia Type 3 Caused by AP2S1 Mutation

Sirpa Tenhola, Geoffrey N. Hendy, Helena Valta, Lucie Canaff, Bonnie S. P. Lee, Betty Y. L. Wong, Matti J. Valimaki, David E. C. Cole, Outi Makitie

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalJournal of Clinical Endocrinology and Metabolism
Volume100
Issue number7
Pages (from-to)2515-2518
Number of pages4
ISSN0021-972X
DOIs
Publication statusPublished - Jul 2015
MoE publication typeA1 Journal article-refereed

Fields of Science

  • LOCALIZATION
  • 3121 Internal medicine
  • 3123 Gynaecology and paediatrics

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