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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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Titel: |
Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene |
Auteur: |
Obermannova, Barbora Banghova, Karolina SumnÃk, Zdenek Dvorakova, Hana M. Betka, Jan Fencl, Filip Kolouskova, Stanislava Cinek, Ondrej Lebl, Jan |
Verschenen in: |
European journal of pediatrics |
Paginering: |
Jaargang 168 (2008) nr. 5 pagina's 569-573 |
Jaar: |
2008 |
Inhoud: |
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Uitgever: |
Springer-Verlag, Berlin/Heidelberg |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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