Biochemical diagnosis of Sanfilippo disorder types A and B

Author:

Nosier Soha S.ORCID,El Nakeeb Seham M.S.,Ibrahim Mona M.,El-Gammal Mona,Fateen Ekram M.

Publisher

Elsevier BV

Subject

Genetics,Biotechnology

Reference46 articles.

1. Incidence and natural history of mucopolysaccharidosis type III in France and comparison with United Kingdom and Greece;He´ron;Am J Med Genet Part A.,2011

2. Neufeld EF and Muenzer J. The mucopolysaccharidoses, in: C.R. Scriver, A.L. Beaudet, W.S. Sly, D. Valle (Eds.), The Metabolic and Molecular Bases of Inherited Disease, 3McGraw-Hill, NewYork, 2001; 3421–3452.

3. A phase I/II study on intracerebroventricular tralesinidase alfa in patients with Sanfilippo syndrome type B;Muschol;J Clin Invest,2023

4. Sanfilippo syndrome: consensus guidelines for clinical care;Muschol;Orphanet J Rare Dis,2022

5. Mucopolysaccharidosis type II: one hundred years of research, diagnosis, and treatment;D’Avanzo;Int J Mol Sci,2020

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