Lysosomal alpha-N-acetylgalactosaminidase deficiency: a new inherited metabolic disease

Lancet. 1987 Oct 3;2(8562):804. doi: 10.1016/s0140-6736(87)92542-6.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Carbohydrate Metabolism, Inborn Errors / genetics*
  • Child, Preschool
  • Hexosaminidases / deficiency*
  • Humans
  • Male
  • alpha-N-Acetylgalactosaminidase

Substances

  • Hexosaminidases
  • NAGA protein, human
  • alpha-N-Acetylgalactosaminidase