2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency is caused by mutations in the HADH2 gene

Open Access
Authors
  • R. Ofman
  • J.P.N. Ruiter
  • M. Feenstra
  • M. Duran
  • B-T. Poll-The
  • J. Zschocke
  • R. Ensenauer
  • W. Lehnert
  • J.O. Sass
  • W. Sperl
  • R.J.A. Wanders
Publication date 2003
Journal American Journal of Human Genetics
Volume | Issue number 72
Pages (from-to) 1300-1307
Organisations
  • Faculty of Medicine (AMC-UvA)
Document type Article
Note Ofman nwp. ©2003 The University of Chicago Press
Published at https://doi.org/10.1086/375116
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