Stray-Pedersen, Asbjørg
Backe, Paul H.
Sorte, Hanne S.
Mørkrid, Lars
Chokshi, Niti Y.
Erichsen, Hans Christian
Gambin, Tomasz
Elgstøen, Katja B.P.
Bjørås, Magnar
Wlodarski, Marcin W.
Krüger, Marcus
Jhangiani, Shalini N.
Muzny, Donna M.
Patel, Ankita
Raymond, Kimiyo M.
Sasa, Ghadir S.
Krance, Robert A.
Martinez, Caridad A.
Abraham, Shirley M.
Speckmann, Carsten
Ehl, Stephan
Hall, Patricia
Forbes, Lisa R.
Merckoll, Else
Westvik, Jostein
Nishimura, Gen
Rustad, Cecilie F.
Abrahamsen, Tore G.
Rønnestad, Arild
Osnes, Liv T.
Egeland, Torstein
Rødningen, Olaug K.
Beck, Christine R.
Boerwinkle, Eric A.
Gibbs, Richard A.
Lupski, James R.
Orange, Jordan S.
Lausch, Ekkehart
Hanson, I. Celine
Funding for this research was provided by:
National Human Genome Research Institute (U54HG003273)
National Human Genome Research Institute (U54HG006542)
Seventh Framework Programme (602300)
Bundesministerium für Bildung und Forschung (01GM1109A)
This article is maintained by: Elsevier
Article Title: PGM3 Mutations Cause a Congenital Disorder of Glycosylation with Severe Immunodeficiency and Skeletal Dysplasia
Journal Title: The American Journal of Human Genetics
CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.ajhg.2014.05.007
Content Type: article
Copyright: Copyright © 2014 The American Society of Human Genetics. Published by Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.