Open AccessLoss of Heterozygosity in Parathyroid Glands of Familial Hypercalcemia with Hypercalciuria and Point Mutation in Calcium Receptor
Author(s) -
E. Szabo
Publication year - 2002
Publication title -
the journal of clinical endocrinology and metabolism/journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.87.8.3961
Subject(s) - hypercalciuria , loss of heterozygosity , calcium sensing receptor , point mutation , endocrinology , medicine , calcium , mutation , parathyroid hormone , biology , genetics , gene , allele