Publication | Open Access
Frequent Germ-Line Mutations of the MEN1, CASR, and HRPT2/CDC73 Genes in Young Patients with Clinically Non-familial Primary Hyperparathyroidism
112
Citations
34
References
2011
Year
Mendelian DisorderGenetic DisorderHrpt2/cdc73 GenesGeneticsParathyroid HormoneParathyroid DiseasePathologyFrequent Germ-line MutationsMolecular GeneticsParathyroid GlandMedicineYoung PatientsClinical Genetics
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