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Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S , which Encode Subcomponents C1r and C1s of Complement

Journal Article published Nov 2016 in The American Journal of Human Genetics volume 99 issue 5 on pages 1005 to 1014

Research funded by Oesterreichische Nationalbank (15408) | Propter Homines Foundation | Austrian Science Fund (W1253-B24) | SNF (310030_138288) | UK MRC Clinical Sciences Centre | Wellcome Clinical Training Fellowship (100565/Z/12/Z) | Freudmann Fund for Translational Research in Ehlers Danlos syndrome, the Ehlers Danlos Research Fund, and the Center for Precision Diagnostics at the University of Washington | National Heart, Lung, and Blood Institute (U54HG006493)

Authors: Ines Kapferer-Seebacher, Melanie Pepin, Roland Werner, Timothy J. Aitman, Ann Nordgren, Heribert Stoiber, Nicole Thielens, Christine Gaboriaud, Albert Amberger, Anna Schossig, Robert Gruber, Cecilia Giunta, Michael Bamshad, Erik Björck, Christina Chen, David Chitayat, Michael Dorschner, Marcus Schmitt-Egenolf, Christopher J. Hale, David Hanna, Hans Christian Hennies, Irene Heiss-Kisielewsky, Anna Lindstrand, Pernilla Lundberg, Anna L. Mitchell, Deborah A. Nickerson, Eyal Reinstein, Marianne Rohrbach, Nikolaus Romani, Matthias Schmuth, Rachel Silver, Fulya Taylan, Anthony Vandersteen, Jana Vandrovcova, Ruwan Weerakkody, Margaret Yang, F. Michael Pope, Peter H. Byers, Johannes Zschocke, Kirk Aleck, Zoltan Banki, Joszef Dudas, Herbert Dumfahrt, Hady Haririan, James K. Hartsfield, Charles N. Kagen, Uschi Lindert, Thomas Meitinger, Wilfried Posch, Christian Pritz, David Ross, Richard J. Schroer, Georg Wick, Robert Wildin, Doris Wilflingseder