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Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene
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Author/s
author: Zdeněk Šumník, Ondrej Cinek, Jan Betka, Jan Lebl, Stanislava Koloušková, Barbora Obermannová, Karolina Banghova, Filip Fencl
Work details
Publication date
August 27, 2008
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Language
English
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