A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents

Open Access
Authors
  • A. Raas-Rothschild
  • R.J.A. Wanders
  • P.A.W. Mooijer
  • J. Gootjes
  • H.R. Waterham
  • A. Gutman
  • Y. Suzuki
  • N. Shimozama
  • N. Kondo
  • G. Eshel
  • M. Espeel
  • F. Roels
  • H. Korman
Publication date 2002
Journal American Journal of Human Genetics
Volume | Issue number 70
Pages (from-to) 1062-1068
Organisations
  • Faculty of Medicine (AMC-UvA)
Document type Article
Note Israel. ©2002 University of Chicago Press
Published at https://doi.org/10.1086/339766
Downloads
Permalink to this page
Back