Skeletal and hematological anomalies in HYAL2‐deficient mice: a second type of mucopolysaccharidosis IX?
Author:
Affiliation:
1. URPhyM, Laboratory of Physiology and PharmacologyUniversity of NamurNamurBelgium
2. Department of Biochemistry and Medical GeneticsThe University of ManitobaWinnipegManitobaCanada
3. Halozyme TherapeuticsSan DiegoCaliforniaUSA
Publisher
Wiley
Subject
Genetics,Molecular Biology,Biochemistry,Biotechnology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.08-111997
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