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The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)

(2010) HUMAN GENETICS. 128(1). p.79-88
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Keywords
INVOLVEMENT, ATP6V0A2, PATHWAY, EHLERS-DANLOS-SYNDROME, MUTATIONS, GENE

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Citation

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Chicago
Syx, Delfien, Fransiska Malfait, Lut Van Laer, JAN HELLEMANS, T Hermanns-Le, Andy Willaert, A Benmansour, Anne De Paepe, and A Verloes. 2010. “The RIN2 Syndrome: a New Autosomal Recessive Connective Tissue Disorder Caused by Deficiency of Ras and Rab Interactor 2 (RIN2).” Human Genetics 128 (1): 79–88.
APA
Syx, D., Malfait, F., Van Laer, L., HELLEMANS, J., Hermanns-Le, T., Willaert, A., Benmansour, A., et al. (2010). The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2). HUMAN GENETICS, 128(1), 79–88.
Vancouver
1.
Syx D, Malfait F, Van Laer L, HELLEMANS J, Hermanns-Le T, Willaert A, et al. The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2). HUMAN GENETICS. NEW YORK: Springer; 2010;128(1):79–88.
MLA
Syx, Delfien et al. “The RIN2 Syndrome: a New Autosomal Recessive Connective Tissue Disorder Caused by Deficiency of Ras and Rab Interactor 2 (RIN2).” HUMAN GENETICS 128.1 (2010): 79–88. Print.
@article{989284,
  author       = {Syx, Delfien and Malfait, Fransiska and Van Laer, Lut and HELLEMANS, JAN and Hermanns-Le, T and Willaert, Andy and Benmansour, A and De Paepe, Anne and Verloes, A},
  issn         = {0340-6717},
  journal      = {HUMAN GENETICS},
  keywords     = {INVOLVEMENT,ATP6V0A2,PATHWAY,EHLERS-DANLOS-SYNDROME,MUTATIONS,GENE},
  language     = {eng},
  number       = {1},
  pages        = {79--88},
  publisher    = {Springer},
  title        = {The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)},
  url          = {http://dx.doi.org/10.1007/s00439-010-0829-0},
  volume       = {128},
  year         = {2010},
}

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