Novel mutation of the calcium sensing receptor gene in familial hypocalciuric hypercalcaemia and neonatal severe hyperparathyroidism [1]

Clinical Endocrinology

Volumn 65, Issue 6, 2006, Pages 826-827

  Caixeta De Andrade, Simone ^a   Kohara, Suely Keiko ^b   D'Souza Li, Lilia ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

^b University of Joinville   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM SENSING RECEPTOR;

DISEASE SEVERITY; FAMILIAL DISEASE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HYPERCALCEMIA; HYPERPARATHYROIDISM; HYPOCALCIURIA; LETTER; NEWBORN DISEASE; PRIORITY JOURNAL;

CALCIUM; CONSANGUINITY; EXONS; HUMANS; HYPERCALCEMIA; HYPERPARATHYROIDISM; INFANT, NEWBORN; MALE; POINT MUTATION; RECEPTORS, CALCIUM-SENSING;

EID: 33751120663     PISSN: 03000664     EISSN: 13652265     Source Type: Journal    
DOI: 10.1111/j.1365-2265.2006.02640.x     Document Type: Letter

References (6)

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