Progressive mental regression in siblings with Morquio disease Type B (mucopolysaccharidosis IV B)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1987.tb03296.x/fullpdf
Reference30 articles.
1. Mor-quio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: mucopolysaccharidosis IV B;Arbisser;Am. J. Med. Genet.,1977
2. Heterogeneity of Morquio disease;Beck;Clin. Genet.,1986
3. Late infantile systemic lipido-sis: major monosialogangliosidosis. Delineation of two types;Derry;Neurology (Minneapolis),1968
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