Heterogeneity of Morquio disease
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1986.tb01262.x/fullpdf
Reference27 articles.
1. Morquio-like syndrome with β-galactosidase deficiency and normal hexosamine sulfatase activity: Mucopolysaccharidosis IV B.;Arbisser;Am. J. Med. Genet.,1977
2. Unusual forms of familial osteochondrodystrophy.;Dale;Acta Radiol.,1931
3. Biochemical defect of non-keratan-sulfate-excreting Morquio syndrome.;Fujimoto;Am. J. Med. Genet.,1983
4. Different properties of residual N-acet-ylgalactosamine-6-sulfate sulfatase in fibroblasts from patients with mild and severe forms of Morquio disease type A.;Glössl;Pediatr. Res.,1981
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