Addendum to “Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency” [Mol. Genet. Metab. 77 (2002) 195–201]

  • 10.1016/s1096-7192(02)00202-0
  • Molecular Genetics and Metabolism
  • p 82-82, Volume 78, Issue 1,
  • journal-article