1.
J Paediatr Child Health
; 45(7-8): 469-72, 2009.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19712183
RESUMO
We report the long-term follow-up of successful treatment of mucopolysaccharidosis type I H (MPS IH, Hurler syndrome) with combined enzyme replacement therapy and haematopoietic progenitor stem cell transplant.