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PPIB Mutations Cause Severe Osteogenesis Imperfecta

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Year: 2009
Type: article
Source: The American Journal of Human Genetics
DOI: 10.1016/j.ajhg.2009.09.001
Authors: Fleur S. van Dijk, Isabel M. Nesbitt, Eline H. Zwikstra, Peter G.J. Nikkels, Sander R. Piersma, Silvina A. Fratantoni, Connie R. Jimenez, Margriet Huizer, Alice C. Morsman, Jan M. Cobben, Mirjam H.H. van Roij, Mariet W. Elting, Jonathan I.M.L. Verbeke, Liliane C.D. Wijnaendts, Nick J. Shaw, Wolfgang Högler, Carole McKeown, Erik A. Sistermans, Ann Dalton, Hanne Meijers-Heijboer, Gerard Pals
Institutions: Amsterdam UMC Location Vrije Universiteit Amsterdam, Sheffield Children's NHS Foundation Trust, Sheffield Children's Hospital, University Medical Center Utrecht, Amsterdam UMC Location University of Amsterdam, Emma Kinderziekenhuis, Birmingham Children's Hospital, Birmingham Women's Hospital
Language: English

Topic: Connective tissue disorders research
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: bronze
OpenAlex ID: W2016252499
FWCI: 11.87
Cites: 20
Cited by: 302
Related to: 10
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