Molecular genetics of mucopolysaccharidosis type IIIA and IIIB: Diagnostic, clinical, and biological implications-Reference-Cited by-同舟云学术

Molecular genetics of mucopolysaccharidosis type IIIA and IIIB: Diagnostic, clinical, and biological implications

Published:2001-10 Issue:4 Volume:18 Page:264-281
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Yogalingam Gouri,Hopwood John J.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference53 articles.

1. Canine Heparan Sulfate Sulfamidase and the Molecular Pathology Underlying Sanfilippo Syndrome Type A in Dachshunds

2. 2000b. Sanfilippo syndrome type B in emu (Dromaius novaehollandiae). International Symposium on Innovative Therapies and 6th International Symposium on Mucopolysaccharidosis and Related Diseases, 2000, May 19-21, Minneapolis, Minnesota, A6.

3. Behaviour in mucopolysaccharide disorders.

4. Identification of 12 novel mutations in the alpha-N-acetylglucosaminidase gene in 14 patients with Sanfilippo syndrome type B (mucopolysaccharidosis type IIIB).

5. Mutational analysis of Sanfilippo syndrome type A (MPS IIIA): identification of 13 novel mutations

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