首页 | 本学科首页   官方微博 | 高级检索  
     


Albright hereditary osteodystrophy: report of a particular clinical phenotype caused by a novel GNAS mutation
Authors:F Alvarez  ML Kottler  C Paul  I Gennero  JP Salles  J Mazereeuw‐Hautier
Affiliation:1. Department of Dermatology, H?pital Purpan, CHU de Toulouse, 31059 Toulouse Cedex 9, France;2. Laboratory of Molecular Genetics and Reference Center for Rare Disorders of Ca et P metabolism, CHU Clémenceau, avenue G. Clémenceau, BP 95182, 14033 Caen Cedex 5, France;3. INSERM Unit 563;4. Université Paul Sabatier Toulouse III;5. H?pital Purpan, CHU de Toulouse 31059, Toulouse Cedex 9, France;6. Biochemistry, Institut de Biologie, CHU de Toulouse 31059, Toulouse, Cedex 9, France;7. Unit of Endocrinology and Bone Diseases, H?pital des Enfants, TSA 70034 CHU de Toulouse 31059, Toulouse, Cedex 9, France
Abstract:
Keywords:
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号