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Bi-allelic AEBP1 mutations in two patients with Ehlers-Danlos syndrome

(2019) HUMAN MOLECULAR GENETICS. 28(11). p.1853-1864
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Chicago
Syx, Delfien, Inge De Wandele, Sofie Symoens, Riet De Rycke, Olivier Hougrand, Nicol Voermans, Anne De Paepe, and Fransiska Malfait. 2019. “Bi-allelic AEBP1 Mutations in Two Patients with Ehlers-Danlos Syndrome.” Human Molecular Genetics 28 (11): 1853–1864.
APA
Syx, D., De Wandele, I., Symoens, S., De Rycke, R., Hougrand, O., Voermans, N., De Paepe, A., et al. (2019). Bi-allelic AEBP1 mutations in two patients with Ehlers-Danlos syndrome. HUMAN MOLECULAR GENETICS, 28(11), 1853–1864.
Vancouver
1.
Syx D, De Wandele I, Symoens S, De Rycke R, Hougrand O, Voermans N, et al. Bi-allelic AEBP1 mutations in two patients with Ehlers-Danlos syndrome. HUMAN MOLECULAR GENETICS. 2019;28(11):1853–64.
MLA
Syx, Delfien et al. “Bi-allelic AEBP1 Mutations in Two Patients with Ehlers-Danlos Syndrome.” HUMAN MOLECULAR GENETICS 28.11 (2019): 1853–1864. Print.
@article{8619953,
  author       = {Syx, Delfien and De Wandele, Inge and Symoens, Sofie and De Rycke, Riet and Hougrand, Olivier and Voermans, Nicol and De Paepe, Anne and Malfait, Fransiska},
  issn         = {0964-6906},
  journal      = {HUMAN MOLECULAR GENETICS},
  language     = {eng},
  number       = {11},
  pages        = {1853--1864},
  title        = {Bi-allelic AEBP1 mutations in two patients with Ehlers-Danlos syndrome},
  url          = {http://dx.doi.org/10.1093/hmg/ddz024},
  volume       = {28},
  year         = {2019},
}

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