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Identification and Functional Characterization of IDS Gene Mutations Underlying Taiwanese Hunter Syndrome (Mucopolysaccharidosis Type II).
Lin, Hsiang-Yu; Tu, Ru-Yi; Chern, Schu-Rern; Lo, Yun-Ting; Fran, Sisca; Wei, Fang-Jie; Huang, Sung-Fa; Tsai, Shin-Yu; Chang, Ya-Hui; Lee, Chung-Lin; Lin, Shuan-Pei; Chuang, Chih-Kuang.
Afiliação
  • Lin HY; Department of Medical Research, MacKay Memorial Hospital, New Taipei City 25160, Taiwan.
  • Tu RY; Department of Pediatrics, MacKay Memorial Hospital, Taipei 10449, Taiwan.
  • Chern SR; MacKay Junior College of Medicine, Nursing and Management, New Taipei City 25245, Taiwan.
  • Lo YT; Department of Medicine, MacKay Medical College, New Taipei City 25245, Taiwan.
  • Fran S; Department of Medical Research, China Medical University Hospital, China Medical University, Taichung 40402, Taiwan.
  • Wei FJ; Rare Disease Center, MacKay Memorial Hospital, Taipei 10449, Taiwan.
  • Huang SF; Department of Medical Research, MacKay Memorial Hospital, New Taipei City 25160, Taiwan.
  • Tsai SY; Department of Medical Research, MacKay Memorial Hospital, New Taipei City 25160, Taiwan.
  • Chang YH; Rare Disease Center, MacKay Memorial Hospital, Taipei 10449, Taiwan.
  • Lee CL; Department of Medical Research, MacKay Memorial Hospital, New Taipei City 25160, Taiwan.
  • Lin SP; Department of Medical Research, MacKay Memorial Hospital, New Taipei City 25160, Taiwan.
  • Chuang CK; Department of Laboratory Medicine, MacKay Memorial Hospital, New Taipei City 25160, Taiwan.
Int J Mol Sci ; 21(1)2019 Dec 23.
Article em En | MEDLINE | ID: mdl-31877959
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glicoproteínas / Mucopolissacaridose II / Mutação de Sentido Incorreto Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Infant / Male País como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glicoproteínas / Mucopolissacaridose II / Mutação de Sentido Incorreto Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Infant / Male País como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article