Unusually severe phenotype of neonatal primary...

European Journal of Pediatrics 2009 / 05 Vol. 168; Iss. 5

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

Barbora Obermannova, Karolina Banghova, Zdenek Sumník, Hana M. Dvorakova, Jan Betka, Filip Fencl, Stanislava Kolouskova, Ondrej Cinek, Jan Lebl
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Volume:
168
Language:
english
Pages:
5
DOI:
10.1007/s00431-008-0794-y
Date:
May, 2009
File:
PDF, 126 KB
english, 2009
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