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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

Data up to Jan 2025

Published1999
Citations201
References26

Total Citations Per Year

Abstract

References (26)

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Mutations in HYAL1 , a member of a tandemly distributed multigene family encoding… (1999) – Proceedings of the National Academy of Sciences | Metascience Observatory Explorer