Work

Distinct OI phenotype caused by COL1 C-proteinase site mutations

Year: 2009

Type: article

Source: Bone

DOI: 10.1016/j.bone.2009.03.152

Authors: A.M. Barnes, K. Lindahl, M.P. Whyte, T. Hefferan, C. Rubin, A. Kindmark, W. McAlister, S. Mumm, O. Ljunggren, J.C. Marini⁎

Institutions: National Institutes of Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Uppsala University, Shriners Hospitals for Children - St. Louis, Mayo Clinic

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: closed

OpenAlex ID: W1990425113

FWCI:

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