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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: Jan Betka  Q112372928  Jan Lebl  Zdeněk Šumník  Barbora Obermannová  Filip Fencl  Karolina Banghova  Ondrej Cinek 

Publication date August 27, 2008
Language English
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