Hurler's Syndrome: Deficiency of a Specific Beta Galactosidase Isoenzyme-Reference-Cited by-同舟云学术

Hurler's Syndrome: Deficiency of a Specific Beta Galactosidase Isoenzyme

Published:1969-08-08 Issue:3893 Volume:165 Page:611-613
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Ho Mae Wan¹,O'Brien John S.¹

Affiliation:

1. Department of Neurosciences, School of Medicine, University of California at San Diego, La Jolla 92037

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference12 articles.

1. FRANTANTONI, J.C., PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 60: 699 (1968).

2. LAGUNOFF, D, SITE OF MUCOPOLYSACCHARIDE ACCUMULATION IN HURLERS SYNDROME - AN ELECTRON MICROSCOPIC AND HISTOCHEMICAL STUDY, LABORATORY INVESTIGATION 15: 1578 (1966).

3. LEDEEN, R, STRUCTURE COMPARISON OF MAJOR MONOSIALOGANGLIOSIDES FROM BRAINS OF NORMAL HUMAN GARGOYLISM AND LATE INFANTILE SYSTEMIC LIPIDOSIS .I., JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 24: 341 (1965).

4. MacBrinn, M. C., New England Journal of Medicine 281: 338 (1969).

5. McKusick V. A. Heritable Disorders of Connective Tissue 3 325 (1966).

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