Mucopolysaccharidosis in a Cat with Arylsulfatase B Deficiency: A Model of Maroteaux-Lamy Syndrome-Reference-Cited by-同舟云学术

Mucopolysaccharidosis in a Cat with Arylsulfatase B Deficiency: A Model of Maroteaux-Lamy Syndrome

Published:1977-11-25 Issue:4319 Volume:198 Page:834-836
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Jezyk Peter F.¹,Haskins Mark E.¹,Patterson Donald F.¹,Mellman William J.²,Greenstein Michael²

Affiliation:

1. Section of Medical Genetics, University of Pennsylvania School of Veterinary Medicine, and the University of Pennsylvania Genetics Center, Philadelphia 19174

2. Department of Human Genetics, University of Pennsylvania School of Medicine, Philadelphia 19174

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference30 articles.

1. BELCHER, R.W., ULTRASTRUCTURE AND CYTOCHEMISTRY OF LYMPHOCYTES IN GENETIC MUCOPOLYSACCHARIDOSES, ARCHIVES OF PATHOLOGY 93: 1 (1972).

2. BERATIS, N.G., ARYLSULFATASE B DEFICIENCY IN MAROTEAUX-LAMY SYNDROME - CELLULAR STUDIES AND CARRIER IDENTIFICATION, PEDIATRIC RESEARCH 9: 475 (1975).

3. CIFONELLI, J.A., CHEMISTRY OF BETA-HEPARIN (CHONDROITINSULFURIC ACID-B), JOURNAL OF BIOLOGICAL CHEMISTRY 233: 541 (1958).

4. GM 2 Ganglioside Lysosomal Storage Disease in Cats with α-Hexosaminidase Deficiency

5. COWELL, K.R., MUCOPOLYSACCHARIDOSIS IN A CAT, JOURNAL OF THE AMERICAN VETERINARY MEDICAL ASSOCIATION 169: 334 (1976).

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