Fibrillin-1 Mutations Causing Weill-Marchesani Syndrome and Acromicric and Geleophysic Dysplasias Disrupt Heparan Sulfate Interactions

Open Access

Peer-reviewed

Research Article

Stuart A. Cain ,

* E-mail: stuart.a.cain@manchester.ac.uk

Affiliation Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom
⨯
Amanda McGovern,

Affiliation Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom
⨯
Andrew K. Baldwin,

Affiliation Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom
⨯
Clair Baldock,

Affiliation Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom
⨯
Cay M. Kielty

Affiliation Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom
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Heparin
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Point mutation
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Deletion mutation
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Binding analysis
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Monomers
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Protein domains
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Cell binding
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Weill-Marchesani syndrome
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