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Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation by Willaert, A. (author);Malfait, F. (author);Symoens, S. (author);Gevaert, K. (author);Kayserili, H. (author);Megarbane, A. (author);Mortier, G. (author);Leroy, J. G. (author);Coucke, P. J. (author);De Paepe, A. (author) is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Willaert, A. (author);Malfait, F. (author);Symoens, S. (author);Gevaert, K. (author);Kayserili, H. (author);Megarbane, A. (author);Mortier, G. (author);Leroy, J. G. (author);Coucke, P. J. (author);De Paepe, A. (author)
Publisher
BMJ Publishing Group; BMJ (ISSN 0022-2593)
Published
2008
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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