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Diagnosing lysosomal storage disorders: mucopolysaccharidosis type II

Britt A Johnson1, Otto P van Diggelen2,3, Angela Dajnoki1

  • 1Division of Clinical and Translational Genetics, Dr. John T. MacDonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida.

Current Protocols in Human Genetics
|February 11, 2014
PubMed

Keywords:
Hunter SyndromeMPS IIalpha-iduronate-2-sulfatasedried blood spotfluorometryglycosaminoglycansmucopolysaccharidemucopolysaccharidosis Type II

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