A glycogene mutation map for discovery of diseases of glycosylation-Reference-Cited by-同舟云学术

A glycogene mutation map for discovery of diseases of glycosylation

Published:2014-09-28 Issue:2 Volume:25 Page:211-224
ISSN:0959-6658
Container-title:Glycobiology
language:en
Short-container-title:

Author:

Hansen Lars¹,Lind-Thomsen Allan²,Joshi Hiren J¹,Pedersen Nis Borbye¹,Have Christian Theil³,Kong Yun¹,Wang Shengjun¹,Sparso Thomas³,Grarup Niels³,Vester-Christensen Malene Bech¹,Schjoldager Katrine¹,Freeze Hudson H⁴,Hansen Torben³,Pedersen Oluf³,Henrissat Bernard¹⁵,Mandel Ulla¹,Clausen Henrik¹,Wandall Hans H¹,Bennett Eric P¹

Affiliation:

1. Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, School of Dentistry, Faculty of Health Sciences

2. Wilhelm Johannsen Center for Genome Research, Department of Cellular and Molecular Medicine, Faculty of Health Sciences, University of Copenhagen, Blegdamsvej 3B, Copenhagen N DK-2200, Denmark

3. The Novo Nordisk Foundation Center for Basic Metabolic Research, Metabolics Genetics, Universitetsparken, Copenhagen Ø DK-2100, Denmark

4. Human Genetics Program, Sanford Children's Health Research Center, Sanford Burnham Medical Research Institute, La Jolla, CA 92037, USA

5. Architecture et Fonction des Macromolécules Biologiques, UMR 7257, Centre National de la Recherche Scientifique, Aix-Marseille Université, Marseille 13288, France

Funder

the University of Copenhagen, The Danish National Research Foundation

Rocket Fund

Publisher

Oxford University Press (OUP)

Subject

Biochemistry

Link

http://academic.oup.com/glycob/article-pdf/25/2/211/16657828/cwu104.pdf

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2. Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes;Albrechtsen;Diabetologia,2013