Sanfilippo syndrome: Overall review

Author:

Andrade Fernando1,Aldámiz-Echevarría Luis1,Llarena Marta1,Couce María Luz2

Affiliation:

1. Division of Metabolism; BioCruces Health Research Institute, CIBER de Enfermedades Raras (CIBERER); Barakaldo Spain

2. Unit of Diagnosis and Treatment of Congenital Metabolic Diseases; Neonatology Service, Department of Pediatrics, CIBER de Enfermedades Raras (CIBERER), IDIS Clinic University Hospital of Santiago de Compostela; Coruña Spain

Publisher

Wiley

Subject

Pediatrics, Perinatology, and Child Health

Reference78 articles.

1. Mucopolysaccharides disorder: A possible new genotype of Hurler's syndrome;Harris;Am. J. Dis. Child.,1961

2. Mental retardation associated with acid mucopolysacchariduria (heparitin sulfate type);Sanfilippo;J. Pediatr.,1963

3. Sanfilippo syndrome: A mini-review;Valstar;J. Inherit. Metab. Dis.,2008

4. Incidence of the mucopolysaccharidoses in Western Australia;Nelson;Am. J. Med. Genet. A,2003

5. The frequency of lysosomal storage diseases in The Netherlands;Poorthuis;Hum. Genet.,1999

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