Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene

Published 2008 View Full Article

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Title
Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene
Authors
Keywords
-
Journal
EUROPEAN JOURNAL OF PEDIATRICS
Volume 168, Issue 5, Pages 569-573
Publisher
Springer Nature
Online
2008-08-26
DOI
10.1007/s00431-008-0794-y

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