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Compound heterozygous mutations of the TNXB gene cause primary myopathy

(2013) NEUROMUSCULAR DISORDERS. 23(8). p.664-669
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ABNORMALITIES, MUSCLE, COLLAGEN, MODEL, SUPPORT OVERLAP, CONGENITAL MUSCULAR-DYSTROPHY, Myopathy, Extracellular matrix, TENASCIN-X DEFICIENCY, EHLERS-DANLOS-SYNDROME, Connective tissue disorders, Ehlers-Danlos syndrome, Tenascin-X

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Citation

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MLA
Pénisson-Besnier, Isabelle, Valérie Allamand, Philippe Beurrier, et al. “Compound Heterozygous Mutations of the TNXB Gene Cause Primary Myopathy.” NEUROMUSCULAR DISORDERS 23.8 (2013): 664–669. Print.
APA
Pénisson-Besnier, I., Allamand, V., Beurrier, P., Martin, L., Schalkwijk, J., van Vlijmen-Willems, I., Gartioux, C., et al. (2013). Compound heterozygous mutations of the TNXB gene cause primary myopathy. NEUROMUSCULAR DISORDERS, 23(8), 664–669.
Chicago author-date
Pénisson-Besnier, Isabelle, Valérie Allamand, Philippe Beurrier, Ludovic Martin, Joost Schalkwijk, Ivonne van Vlijmen-Willems, Corine Gartioux, et al. 2013. “Compound Heterozygous Mutations of the TNXB Gene Cause Primary Myopathy.” Neuromuscular Disorders 23 (8): 664–669.
Chicago author-date (all authors)
Pénisson-Besnier, Isabelle, Valérie Allamand, Philippe Beurrier, Ludovic Martin, Joost Schalkwijk, Ivonne van Vlijmen-Willems, Corine Gartioux, Fransiska Malfait, Delfien Syx, Laurent Macchi, Pascale Marcorelles, Brigitte Arbeille, Anne Croué, Anne De Paepe, and Frédéric Dubas. 2013. “Compound Heterozygous Mutations of the TNXB Gene Cause Primary Myopathy.” Neuromuscular Disorders 23 (8): 664–669.
Vancouver
1.
Pénisson-Besnier I, Allamand V, Beurrier P, Martin L, Schalkwijk J, van Vlijmen-Willems I, et al. Compound heterozygous mutations of the TNXB gene cause primary myopathy. NEUROMUSCULAR DISORDERS. 2013;23(8):664–9.
IEEE
[1]
I. Pénisson-Besnier et al., “Compound heterozygous mutations of the TNXB gene cause primary myopathy,” NEUROMUSCULAR DISORDERS, vol. 23, no. 8, pp. 664–669, 2013.
@article{4226208,
  author       = {Pénisson-Besnier, Isabelle and Allamand, Valérie and Beurrier, Philippe and Martin, Ludovic and Schalkwijk, Joost and van Vlijmen-Willems, Ivonne and Gartioux, Corine and Malfait, Fransiska and Syx, Delfien and Macchi, Laurent and Marcorelles, Pascale and Arbeille, Brigitte and Croué, Anne and De Paepe, Anne and Dubas, Frédéric},
  issn         = {0960-8966},
  journal      = {NEUROMUSCULAR DISORDERS},
  keywords     = {ABNORMALITIES,MUSCLE,COLLAGEN,MODEL,SUPPORT OVERLAP,CONGENITAL MUSCULAR-DYSTROPHY,Myopathy,Extracellular matrix,TENASCIN-X DEFICIENCY,EHLERS-DANLOS-SYNDROME,Connective tissue disorders,Ehlers-Danlos syndrome,Tenascin-X},
  language     = {eng},
  number       = {8},
  pages        = {664--669},
  title        = {Compound heterozygous mutations of the TNXB gene cause primary myopathy},
  url          = {http://dx.doi.org/10.1016/j.nmd.2013.04.009},
  volume       = {23},
  year         = {2013},
}

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