Clinical heterogeneity in infantile galactosialidosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF00441610.pdf
Reference19 articles.
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4. Gehler J, Cantz M, Tolksdorf M, Spranger J, Gilbert E, Drube H (1974) Mucopolysaccharidosis VII: ?-glucuronidase deficiency. Hum Genet 23:149?158
5. Gillan JE, Lowden JA, Gaskin K, Cutz E (1984) Congenital ascites as a presenting sign of lysosomal storage disease. J Pediatr 104:225?231
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