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机译:
Chinese Univ Hong Kong, Prince Wales Hosp, Dept Chem Pathol, Hong Kong, Hong Kong, Peoples R China;
Queen Elizabeth Hosp, Dept Pathol, Hong Kong, Hong Kong, Peoples R China;
Queen Elizabeth Hosp, Dept Pediat, Hong Kong, Hong Kong, Peoples R ChinaPrincess Margaret Hosp, Dept Pathol, Hong Kong, Hong Kong, Peoples R China;
mucopolysaccharidosis; ARSB gene; mutation analysis; MAROTEAUX-LAMY-SYNDROME; ENZYME REPLACEMENT THERAPY; STOP MUTATIONS; TRANSPLANTATION;
机译:Mucopolysaccharidosis type I: identification of novel mutations that cause Hurler/Scheie syndrome in Chinese families.
机译:IDUA gene mutations in mucopolysaccharidosis type-1 patients from two Pakistani inbred families
机译:Mucopolysaccharidosis type II (Hunter disease): 13 gene mutations in 52 Japanese patients and carrier detection in four families
机译:Best Practices for Executive Leadership Succession Planning in Post-cultural Revolution China First-Generational Family Enterprises =文化大革命后中国第一代家族企业执行领导者继任计划的最佳实践
机译:VI型粘多糖贮积病(MPS VI)和分子分析:ARSB基因中已发表变异的审查和分类
机译:a novel type of familial hypercholesterolemia: Double heterozygous mutations in LDL receptor and LDL receptor adaptor protein 1 gene