Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: Mucopolysaccharidosis IVB-Reference-Cited by-同舟云学术

Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: Mucopolysaccharidosis IVB

Published:1977 Issue:2 Volume:1 Page:195-205
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Arbisser Amir I.,Donnelly Kathleen A.,Scott Charles I.,DiFerrante Nicola,Singh Jagat,Stevenson Roger E.,Aylesworth Arthur S.,Howell R. Rodney,Opitz J. M.

Publisher

Wiley

Subject

Genetics (clinical)

Reference34 articles.

1. : The mucopolysaccharidoses. In “Heritable Disorders of Connective Tissue.” St. Louis: CV Mosby, 1972), p 552.

2. : “Bone Dysplasias.” Philadelphia: WB Saunders, 1974, pp 160-165.

3. Morquio's syndrome: Deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfatase

4. N-acetylgalactosamine-6-sulfate sulfatase in man. Absence of the enzyme in Morquio disease.

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