Open AccessIdentification of Somatic Mutations in Parathyroid Tumors Using Whole-Exome Sequencing
Author(s) -
M. Kyle Cromer,
Lee F. Starker,
Murim Choi,
Robert Udelsman,
Carol NelsonWilliams,
Richard P. Lifton,
Tobias Carling
Publication year - 2012
Publication title -
the 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.2012-1743
Subject(s) - exome sequencing , loss of heterozygosity , biology , men1 , exome , germline mutation , cancer research , multiple endocrine neoplasia , primary hyperparathyroidism , mutation , genetics , allele , gene , endocrinology
The underlying molecular alterations causing sporadic parathyroid adenomas that drive primary hyperparathyroidism have not been thoroughly defined.
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