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Novel genes and mechanisms underlying autosomal dominant retinitis pigmentosa and allied retinal dystrophies

(2017)
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(UGent) , (UGent) and (UGent)
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Keywords
Genetics, SF3B2, autosomal dominant retinitis pigmentosa

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Citation

Please use this url to cite or link to this publication:

Chicago
Van Cauwenbergh, Caroline. 2017. “Novel Genes and Mechanisms Underlying Autosomal Dominant Retinitis Pigmentosa and Allied Retinal Dystrophies”. Ghent, Belgium: Ghent University. Faculty of Medicine and Health Sciences.
APA
Van Cauwenbergh, C. (2017). Novel genes and mechanisms underlying autosomal dominant retinitis pigmentosa and allied retinal dystrophies. Ghent University. Faculty of Medicine and Health Sciences, Ghent, Belgium.
Vancouver
1.
Van Cauwenbergh C. Novel genes and mechanisms underlying autosomal dominant retinitis pigmentosa and allied retinal dystrophies. [Ghent, Belgium]: Ghent University. Faculty of Medicine and Health Sciences; 2017.
MLA
Van Cauwenbergh, Caroline. “Novel Genes and Mechanisms Underlying Autosomal Dominant Retinitis Pigmentosa and Allied Retinal Dystrophies.” 2017 : n. pag. Print.
@phdthesis{8514792,
  author       = {Van Cauwenbergh, Caroline},
  keyword      = {Genetics,SF3B2,autosomal dominant retinitis pigmentosa},
  language     = {eng},
  pages        = {225},
  publisher    = {Ghent University. Faculty of Medicine and Health Sciences},
  school       = {Ghent University},
  title        = {Novel genes and mechanisms underlying autosomal dominant retinitis pigmentosa and allied retinal dystrophies},
  year         = {2017},
}