✦ LIBER ✦
Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency
✍ Scribed by Li F. Chan; Louise A. Metherell; Heiko Krude; Colin Ball; Stephen M. P. O'Riordan; Colm Costigan; Sally A. Lynch; Martin O. Savage; Paolo Cavarzere; Adrian J. L. Clark
- Book ID
- 108704381
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 141 KB
- Volume
- 71
- Category
- Article
- ISSN
- 0300-0664
No coin nor oath required. For personal study only.