Associated Papers
A novel intronic mutation and a missense mutation of MEN1 identified in two Chinese families with multiple endocrine neoplasia type 1.
Han B et al.
Journal of Endocrinological Investigation, 2013
Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism.
Howell VM et al.
The Journal of Molecular Diagnostics : Jmd, 2006
A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing.
Cardinal JW et al.
Journal of Medical Genetics, 2005
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