| 1 | HYAL1, MPS9 |
| Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX. | |
| Triggs-Raine B, et al. | |
| Proc Natl Acad Sci U S A 96(11):6296-300. 1999 | |
| 2 | HYAL1, MPS9 |
| Clinical and biochemical manifestations of hyaluronidase deficiency. | |
| Natowicz MR, Short MP, Wang Y, Dickersin GR, Gebhardt MC, Rosenthal DI, Sims KB, Rosenberg AE. | |
| N Engl J Med 335(14):1029-33. No abstract available. 1996 | |