Oral manifestations in patients and dogs with mucopolysaccharidosis Type VII

© 2019 Wiley Periodicals, Inc. Mucopolysaccharidosis Type VII (MPS7, also called β-glucuronidase deficiency or Sly syndrome; MIM 253220) is an extremely rare autosomal recessive lysosomal storage disease, caused by mutations in the GUSB gene. β-glucuronidase (GUSB) is a lysosomal hydrolase involved...

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Main Authors: Piranit N. Kantaputra, Lachlan J. Smith, Margret L. Casal, Chulaluck Kuptanon, Yu Cheng Chang, Sheela Nampoothiri, Apichai Paiyarom, Thanat Veerasakulwong, Objoon Trachoo, James R. Ketudat Cairns, Wannapa Chinadet, Pranoot Tanpaiboon
格式: 雜誌
出版: 2019
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在線閱讀:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060225175&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/63572
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機構: Chiang Mai University

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