Family study of a novel mutation of mucopolysaccharidosis type VI with a severe phenotype and good response to enzymatic replacement therapy Case report

  1. Ley-Martos, M.
  2. Guerrero, J.M.
  3. Lucas-Javato, M.
  4. Remón-García, C.
  5. Raul García-Lozano, J.
  6. Colón, C.
  7. Crujeiras, P.
  8. Rodrigues, D.
  9. Paul-Sánchez, P.
  10. Macher, H.C.
Medicine (United States)

ISSN: 1536-5964 0025-7974

Year of publication: 2018

Volume: 97

Issue: 42

Type: Article

DOI: 10.1097/MD.0000000000012872 GOOGLE SCHOLAR lock_openOpen access editor