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

Source:http://linkedlifedata.com/resource/pubmed/id/10339581

Proc. Natl. Acad. Sci. U.S.A. 1999 May 25 96 11 6296-300

Download in:

View as

Triples

General Info

PMID
10339581