Mutations in HYAL1, a member of a tandemly distributed...

Proceedings of the National Academy of Sciences 1999 / 05 Vol. 96; Iss. 11

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., Salo, T. J., Zhang, H., Wicklow, B. A., Natowicz, M. R.
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
96
Language:
english
Journal:
Proceedings of the National Academy of Sciences
DOI:
10.1073/pnas.96.11.6296
Date:
May, 1999
File:
PDF, 213 KB
english, 1999
Conversion to is in progress
Conversion to is failed