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Three novel and two recurrent mutations of the Norrie disease gene in patients with Norrie syndrome.

(1996) HUMAN MUTATION. 8(1). p.85-88
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Chicago
FUCHS, S, D VANDEPOL, U BEUDT, U KELLNER, Françoise Meire, W BERGER, and A GAL. 1996. “Three Novel and Two Recurrent Mutations of the Norrie Disease Gene in Patients with Norrie Syndrome.” Human Mutation 8 (1): 85–88.
APA
FUCHS, S., VANDEPOL, D., BEUDT, U., KELLNER, U., Meire, F., BERGER, W., & GAL, A. (1996). Three novel and two recurrent mutations of the Norrie disease gene in patients with Norrie syndrome. HUMAN MUTATION, 8(1), 85–88.
Vancouver
1.
FUCHS S, VANDEPOL D, BEUDT U, KELLNER U, Meire F, BERGER W, et al. Three novel and two recurrent mutations of the Norrie disease gene in patients with Norrie syndrome. HUMAN MUTATION. 1996;8(1):85–8.
MLA
FUCHS, S, D VANDEPOL, U BEUDT, et al. “Three Novel and Two Recurrent Mutations of the Norrie Disease Gene in Patients with Norrie Syndrome.” HUMAN MUTATION 8.1 (1996): 85–88. Print.
@article{188886,
  author       = {FUCHS, S and VANDEPOL, D and BEUDT, U and KELLNER, U and Meire, Fran\c{c}oise and BERGER, W and GAL, A},
  issn         = {1059-7794},
  journal      = {HUMAN MUTATION},
  language     = {eng},
  number       = {1},
  pages        = {85--88},
  title        = {Three novel and two recurrent mutations of the Norrie disease gene in patients with Norrie syndrome.},
  volume       = {8},
  year         = {1996},
}