Biochemical diagnosis of Hunter syndrome on Epstein-Barr virus-transformed lymphoblastoid cell lines
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference35 articles.
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Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Cholesterol sulfate is not degraded but does not accumulate in Epstein-Barr virus-transformed lymphoid cells from patients with X-linked ichthyosis;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;1995-10
2. Heterogeneity of DNA and RNA in Hunter patients;Human Genetics;1993-10
3. Biochemical diagnosis of mucopolysaccharidoses: Experience of 297 diagnoses in a 15-year period (1977–1991);Journal of Inherited Metabolic Disease;1993-03
4. Cell-to-cell contact between normal fibroblasts and lymphoblasts deficient in lysosomal enzymes;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;1992-02
5. Arylsulfatases A and B in EBV-transformed lymphoid cell lines: Studies on their molecular forms in cells from patients with inborn sulfatase deficiencies. Comparative diagnostic value of enzymatic assays;Clinica Chimica Acta;1991-10
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