Author:
Kresse H.,Cantz M.,Figura K.,Glössl J.,Paschke E.
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Genetics (clinical),Drug Discovery,Molecular Medicine
Reference59 articles.
1. Aberg A, Mitelman F, Cantz M, Gehler J (1978) Cardiac puncture of fetus with Hurler's disease avoiding abortion of unaffected co-twin. Lancet II:1007–1012
2. Arbisser AI, Donnelly KA, Scott Jr CI, DiFerrante N, Singh J, Stevenson RE, Aylsworth AA, Howell RR (1977) Morquiolike syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity. Am J Med Genet 1:195–205
3. Bach G, Friedman R, Weissmann B, Neufeld EF (1972) The defect in the Hurler and Scheie syndromes: deficiency ofα-L-iduronidase. Proc Natl Acad Sci USA 69:2048–2051
4. Bach G, Eisenberg F, Cantz M, Neufeld EF (1973) The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase. Proc Natl Acad Sci USA 70:2134–2138
5. Basner R, von Figura K, Glössl J, Klein U, Kresse H, Mlekusch W (1979) Multiple deficiency of mucopolysaccharide sulfatases in mucosulfatidosis. Pediat Res 13:1316–1318
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