Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism associated with mutations in the human Ca2+-sensing receptor gene in three Danish families

Author: Schwarz P.   Larsen N. E.   Lønborg Friis I. M.   Lillquist K.   Brown E. M.   Gammeltoft S.  

Publisher: Informa Healthcare

ISSN: 0036-5513

Source: Scandinavian Journal of Clinical and Laboratory Investigation, Vol.60, Iss.3, 2000-06, pp. : 221-228

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Abstract