Mutations in FKBP10 cause both Bruck syndrome and isolated...

American Journal of Medical Genetics Part A 2011 Vol. 155; Iss. 6

Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans

Ranad Shaheen, Mohammed Al-Owain, Eissa Faqeih, Nadia Al-Hashmi, Ali Awaji, Zayed Al-Zayed, Fowzan S Alkuraya
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Volume:
155
Year:
2011
Language:
english
Pages:
5
DOI:
10.1002/ajmg.a.34025
File:
PDF, 3.12 MB
english, 2011
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