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 |
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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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