✦ LIBER ✦
An Atypical Case of Familial Glucocorticoid Deficiency without Pigmentation Caused by Coexistent Homozygous Mutations in MC2R (T152K) and MC1R (R160W)
✍ Scribed by Turan, S.; Hughes, C.; Atay, Z.; Guran, T.; Haliloglu, B.; Clark, A. J. L.; Bereket, A.; Metherell, L. A.
- Book ID
- 111927113
- Publisher
- Endocrine Society
- Year
- 2012
- Tongue
- English
- Weight
- 180 KB
- Volume
- 97
- Category
- Article
- ISSN
- 0021-972X
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