✦ LIBER ✦
A Disruptive Mutation in Exon 3 of the GNAS Gene with Albright Hereditary Osteodystrophy, Normocalcemic Pseudohypoparathyroidism, and Selective Long Transcript Variant Gsα-L Deficiency
✍ Scribed by Thiele, Susanne; Werner, Ralf; Ahrens, Wiebke; Hoppe, Ute; Marschke, Christine; Staedt, Pia; Hiort, Olaf
- Book ID
- 124162644
- Publisher
- Endocrine Society
- Year
- 2007
- Tongue
- English
- Weight
- 171 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0021-972X
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