Mutations in HYAL1, a Member of a Tandemly Distributed Multigene Family Encoding Disparate Hyaluronidase Activities, Cause a Newly Described Lysosomal Disorder, Mucopolysaccharidosis IX
Proceedings of the National Academy of Sciences of the United States of America - United States
doi 10.1073/pnas.96.11.6296
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May 25, 1999
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Proceedings of the National Academy of Sciences