Missense Mutations in the Melanocortin 2 Receptor Accessory...

Missense Mutations in the Melanocortin 2 Receptor Accessory Protein That Lead to Late Onset Familial Glucocorticoid Deficiency Type 2

Hughes, C. R., Chung, T. T., Habeb, A. M., Kelestimur, F., Clark, A. J. L., Metherell, L. A.
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Volume:
151
Language:
english
Journal:
Endocrinology
DOI:
10.1210/endo.151.6.9991
Date:
June, 2010
File:
PDF, 70 KB
english, 2010
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