Early HSCT corrects the skeleton in MPS.

Published

Journal Article

In this issue of Blood, Pievani et al have identified a potential solution to the remaining barrier to the success of hematopoietic stem cell transplantation (HSCT) in children with severe phenotype Hurler syndrome (mucopolysaccharidosis type I [MPS I]).

Full Text

Duke Authors

Cited Authors

  • Kurtzberg, J

Published Date

  • March 5, 2015

Published In

Volume / Issue

  • 125 / 10

Start / End Page

  • 1518 - 1519

PubMed ID

  • 25745184

Pubmed Central ID

  • 25745184

Electronic International Standard Serial Number (EISSN)

  • 1528-0020

Digital Object Identifier (DOI)

  • 10.1182/blood-2014-11-606681

Language

  • eng

Conference Location

  • United States