- Title
- Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans
- Creators - without role
- Ranad Shaheen - Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi ArabiaMohammed Al-Owain - Alfaisal UniversityEissa Faqeih - King Fahd Medical CityNadia Al-Hashmi - King Faisal Specialist Hospital & Research CentreAli Awaji - King Fahad Central HospitalZayed Al-Zayed - King Faisal Specialist Hospital & Research CentreFowzan S Alkuraya - King Faisal Specialist Hospital & Research Centre
- Publication Details
- American Journal of Medical Genetics Part A, Vol.155A(6), pp.1448-1452
- Publisher
- Wiley Subscription Services, Inc., A Wiley Company; Hoboken
- Number of pages
- 5
- Identifiers
- 9913495508331
- Academic Unit
- King Khalid University; King Faisal University; King Saud University; Alfaisal University
- Language
- English
- Resource Type
- Report
Report
Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans
American Journal of Medical Genetics Part A, Vol.155A(6), pp.1448-1452
Wiley Subscription Services, Inc., A Wiley Company
06/2011
Metrics
1 Record Views