- About this Journal ·
- Abstracting and Indexing ·
- Aims and Scope ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
Case Reports in Neurological Medicine
Volume 2013 (2013), Article ID 254950, 3 pages
Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy
1Latvian Biomedical Research and Study Centre, Ratsupites Street 1, Riga 1067, Latvia
2Children Clinical University Hospital, Medical Genetics Clinic, Riga 1004, Latvia
3Pauls Stradins Clinical University Hospital, Riga 1002, Latvia
4Children Clinical University Hospital, Neurology Clinic, Riga 1004, Latvia
Received 28 May 2013; Accepted 18 July 2013
Academic Editors: D. B. Fee, F. C. Henderson, and J. C. Kattah
Copyright © 2013 Baiba Lace et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
- J. R. W. Yates and A. E. H. Emery, “A population study of adult onset limb-girdle muscular dystrophy,” Journal of Medical Genetics, vol. 22, no. 4, pp. 250–257, 1985.
- X. Q. Rosales, S. J. Moser, T. Tran et al., “Cardiovascular magnetic resonance of cardiomyopathy in limb girdle muscular dystrophy 2B and 2I,” Journal of Cardiovascular Magnetic Resonance, vol. 13, no. 1, article 39, 2011.
- D. Hicks, A. Sarkozy, N. Muelas et al., “A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy,” Brain, vol. 134, no. 1, pp. 171–182, 2011.
- H. Gundesli, B. Talim, P. Korkusuz et al., “Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy,” American Journal of Human Genetics, vol. 87, no. 6, pp. 834–841, 2010.
- S. H. Laval and K. M. D. Bushby, “Limb-girdle muscular dystrophies—from genetics to molecular pathology,” Neuropathology and Applied Neurobiology, vol. 30, no. 2, pp. 91–105, 2004.
- S. A. Greenberg, M. Salajegheh, D. P. Judge et al., “Etiology of limb girdle muscular dystrophy 1D/1E determined by laser capture microdissection proteomics,” Annals of Neurology, vol. 71, no. 1, pp. 141–145, 2012.
- M. B. Harms, R. B. Sommerville, P. Allred et al., “Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy,” Annals of Neurology, vol. 71, no. 3, pp. 407–416, 2012.
- G. M. Rayan and J. J. Tomasek, “Generation of contractile force by cultured Dupuytren's Disease and normal palmar fibroblasts,” Tissue and Cell, vol. 26, no. 5, pp. 747–756, 1994.
- K. E. Kamm and J. T. Stull, “Dedicated Myosin Light Chain Kinases with Diverse Cellular Functions,” Journal of Biological Chemistry, vol. 276, no. 7, pp. 4527–4530, 2001.
- S. Hindocha, D. A. McGrouther, and A. Bayat, “Epidemiological evaluation of dupuytren's disease incidence and prevalence rates in relation to etiology,” Hand, vol. 4, no. 3, pp. 256–269, 2009.
- D. C. Ross, “Epidemiology of Dupuytren's disease,” Hand Clinics, vol. 15, no. 1, pp. 53–62, 1999.
- L. Michou, J.-L. Lermusiaux, J.-P. Teyssedou, T. Bardin, J. Beaudreuil, and E. Petit-Teixeira, “Genetics of Dupuytren's disease,” Joint Bone Spine, vol. 79, no. 1, pp. 7–12, 2012.
- F. Z. Hu, A. Nystrom, A. Ahmed et al., “Mapping of an autosomal dominant gene for Dupuytren's contracture to chromosome 16q in a Swedish family,” Clinical Genetics, vol. 68, no. 5, pp. 424–429, 2005.
- B. Shih, S. Watson, and A. Bayat, “Whole genome and global expression profiling of Dupuytren's disease: systematic review of current findings and future perspectives,” Annals of the Rheumatic Diseases, vol. 71, no. 9, pp. 1440–1447, 2012.