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Compound heterozygous mutations of the TNXB gene cause primary myopathy: response

(2014) NEUROMUSCULAR DISORDERS. 24(1). p.89-89
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Citation

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Chicago
Allamand, Valérie, Philippe Beurrier, Ludovic Martin, Fransiska Malfait, Delfien Syx, and Anne De Paepe. 2014. “Compound Heterozygous Mutations of the TNXB Gene Cause Primary Myopathy: Response.” Neuromuscular Disorders 24 (1): 89–89.
APA
Allamand, V., Beurrier, P., Martin, L., Malfait, F., Syx, D., & De Paepe, A. (2014). Compound heterozygous mutations of the TNXB gene cause primary myopathy: response. NEUROMUSCULAR DISORDERS, 24(1), 89–89.
Vancouver
1.
Allamand V, Beurrier P, Martin L, Malfait F, Syx D, De Paepe A. Compound heterozygous mutations of the TNXB gene cause primary myopathy: response. NEUROMUSCULAR DISORDERS. 2014;24(1):89–89.
MLA
Allamand, Valérie, Philippe Beurrier, Ludovic Martin, et al. “Compound Heterozygous Mutations of the TNXB Gene Cause Primary Myopathy: Response.” NEUROMUSCULAR DISORDERS 24.1 (2014): 89–89. Print.
@article{4346959,
  author       = {Allamand, Valérie and Beurrier, Philippe and Martin, Ludovic and Malfait, Fransiska and Syx, Delfien and De Paepe, Anne},
  issn         = {0960-8966},
  journal      = {NEUROMUSCULAR DISORDERS},
  language     = {eng},
  number       = {1},
  pages        = {89--89},
  title        = {Compound heterozygous mutations of the TNXB gene cause primary myopathy: response},
  url          = {http://dx.doi.org/10.1016/j.nmd.2013.10.008},
  volume       = {24},
  year         = {2014},
}

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