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| Title: | Autosomal Recessive Dilated Cardiomyopathy due to DOLK Mutations Results from Abnormal Dystroglycan O-Mannosylation. |
| Author(s): | Lefeber, D.J. (298210169) Brouwer, A.P.M. de (236446894) Morava, E. (298976846) Riemersma, M. Schuurs-Hoeijmakers, J.H.M. (329215310) Absmanner, B. Verrijp, K. (29897925X) Akker, W.M.R. van den Huijben, K. Steenbergen, G.C. (298203790) Reeuwijk, J. van (315067314) Jozwiak, A. Zucker, N. Lorber, A. Lammens, M.M.Y. (20243222X) Knopf, C. Bokhoven, H. van (11529077X) Grunewald, S. Lehle, L. Kapusta, L. (241976634) Mandel, H. Wevers, R.A. (068311508) |
| Publication year: | 2011 |
| Document type: | Article / Letter to editor |
| Journal: | PLoS Genetics |
| ISSN: | 1553-7390 |
| Volume: | vol. 7 |
| Issue: | iss. 12 |
| Start page: | p. e1002427 |
| End page: | p. e1002427 |
| Subject: | DCN 2: Functional Neurogenomics
IGMD 9: Renal disorder DCN 3: Neuroinformatics IGMD 1: Functional imaging IGMD 3: Genomic disorders and inherited multi-system disorders IGMD 4: Glycostation disorders NCMLS 3A: Genetics and epigenetic pathways of disease NCMLS 3A: Genetics and epigenetic pathways of disease
DCN 2: Functional Neurogenomics NCMLS 3A: Genetics and epigenetic pathways of disease
IGMD 3: Genomic disorders and inherited multi-system disorders ONCOL 3: Translational research
IGMD 9: Renal disorder |
| Organization: | Neurology Laboratory of Genetic, Endocrine and Metabolic Diseases Human Genetics Paediatrics UMCN Extern Pathology |
| Appears in Collections: | Academic bibliography
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Please use this identifier to cite or link to this item:
http://hdl.handle.net/2066/96663
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