Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX-Reference-Cited by-同舟云学术

Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX

Published:1999-05-25 Issue:11 Volume:96 Page:6296-6300
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Triggs-Raine B.,Salo T. J.,Zhang H.,Wicklow B. A.,Natowicz M. R.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference24 articles.

1. Hyaluronidases - a group of neglected enzymes

2. The Hyaluronidases: A Chemical, Biological and Clinical Overview.

3. Hyaluronan: clinical perspectives of an old polysaccharide

4. Hyaluronan in morphogenesis

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