@article{c4736d5e202e4239b75e64b465bec36f,
title = "The Hurler and Hunter syndromes",
abstract = "Since the demonstration that acid mucopolysaccharides accumulate in tissue and urines of patients with the Hurler and Hunter syndromes, other mucopolysaccharidoses have been described. Some lipid storage diseases have also been shown to have an increase in acid mucopolysaccharide with the lipid material stored. Tissue culture technics have shed some light on several aspects of these diseases especially with regard to genetic counselling. Available information is reviewed in an attempt to reconcile current knowledge in arriving at a unifying hypothesis.",
author = "Albert Dorfman and Reuben Matalon",
note = "Funding Information: * Fro111 the Departments of Pediatrics and Biochemistry, LaRabida-University of Chicago Institute, and the \textasciitilde{}trsc\textasciitilde{}ph I{\textquoteright}. Kennedy. Jr. Mental Retardation Research Center, University of Chicago, Chicago, Illinois 60637. {\textquoteleft}This \textbackslash{}\textasciitilde{}ork IY\textasciitilde{}S suppol.tcd by grants from U. S. Public Health Service (AM-05996 and FR 00305), the Illinois and Cllicago lIeart Associations and the Cystic Fibrosis Foundation. Requests for reprints should be adtll-es\& to lh .\textbackslash{}llxw Dorfman, Department of Pediatrics, University of Chicago, 950 East 59th Street, Chicago, Illinois 60637. i Joseph P. Kennedy, Jr. Scholar.",
year = "1969",
month = nov,
doi = "10.1016/0002-9343(69)90164-8",
language = "English (US)",
volume = "47",
pages = "691--707",
journal = "The American Journal of Medicine",
issn = "0002-9343",
publisher = "Elsevier Inc.",
number = "5",
}