Case of a Mongolian child with extensive Mongolian spots in mucopolysaccharidosis type VI: identification of a novel mutation in the arylsulfatase B gene

J Dermatol. 2013 Sep;40(9):758-9. doi: 10.1111/1346-8138.12237. Epub 2013 Jul 16.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child
  • Humans
  • Male
  • Mongolia
  • Mucopolysaccharidosis VI / genetics*
  • Mutation, Missense
  • N-Acetylgalactosamine-4-Sulfatase / genetics*

Substances

  • N-Acetylgalactosamine-4-Sulfatase