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Mutations in HYAL1, a Member of a Tandemly Distributed Multigene Family Encoding Disparate Hyaluronidase Activities, Cause a Newly Described Lysosomal Disorder, Mucopolysaccharidosis IX
Barbara Triggs-Raine, Timothy J. Salo, Hong Zhang, Brandy A. Wicklow and Marvin R. NatowiczVolume:
96
Language:
english
Journal:
Proceedings of the National Academy of Sciences of the United States of America
DOI:
10.2307/47864
Date:
May, 1999
File:
PDF, 1.07 MB
english, 1999