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Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfecta
scientific article
Author/s
author: Jinoh Kim, Oliver Semler, David J Amor, Stefan Bohlander, Bernd Wollnik, Filippo Beleggia, Ravi Savarirayan
Work details
Publication date
February 12, 2015
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Language
English
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