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Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in theCASRgene

✍ Scribed by Barbora Obermannova; Karolina Banghova; Zdenek Sumník; Hana M. Dvorakova; Jan Betka; Filip Fencl; Stanislava Kolouskova; Ondrej Cinek; Jan Lebl

Book ID: 106121632
Publisher: Springer
Year: 2008
Tongue: English
Weight: 126 KB
Volume: 168
Category: Article
ISSN: 0340-6997
DOI: 10.1007/s00431-008-0794-y

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