Absence of alpha-L-iduronidase activity in various tissues from two sibs affected with presumably the Hurler-Scheie compound syndrome

Saved in:
Bibliographic Details
Published inBirth defects original article series Vol. 11; no. 6; p. 341
Main Authors Thompson, J N, Finley, S C, Lorincz, A E, Finley, W H
Format Journal Article
LanguageEnglish
Published United States 1975
Subjects
Adolescent
Adult
Female
Fibroblasts - enzymology
Glycoside Hydrolases - deficiency
Glycoside Hydrolases - metabolism
Humans
Iduronidase - deficiency
Mucopolysaccharidoses - enzymology
Mucopolysaccharidosis I - enzymology
Mucopolysaccharidosis I - genetics
Pregnancy
Skin - enzymology
Online AccessGet more information

Cover

More Information
ISSN:0547-6844