Reference values of serum IgA subclasses in caucasian adults by immunonephelometry.
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چکیده
References 1. Kappas A, Sassa S, Galbraith RA, Nordmann Y. The porphyrias. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The metabolic and molecular bases of inherited diseases, 7th ed. New York: McGraw-Hill, 1995:2103–60. 2. Wassif WS, Deacon AC, Floderus Y, Thunell S, Peters TJ. Acute intermittent porphyria: diagnostic conundrums. Eur J Clin Chem Clin Biochem 1994;32:915–21. 3. Mustajoki P, Tenhunen R. Variant of acute intermittent porphyria with normal erythrocyte uroporphyrinogen-I-synthase activity. Eur J Clin Investig 1985;15:281–4. 4. Krawczak M, Cooper DN. The Human Gene Mutation Database. Trends Genet 1997;13: 121–2. 5. Gu XF, de Rooij F, Lee JS, Te Velde K, Deybach JC, Nordmann Y, et al. High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyria. Hum Genet 1993;91:129– 30. 6. Lee JS, Anvret M. Identification of the most common mutation within the porphobilinogen deaminase gene in Swedish patients with acute intermittent porphyria. Proc Natl Acad Sci U S A 1991;88:10912–5. 7. Kauppinen R. Single-strand conformation polymorphism (SSCP) analysis applied to the diagnosis of acute intermittent porphyria. Mol Cell Probes 1992;6:527–30. 8. Schreiber WE, Fong F, Nassar BA, Jamani A. Heteroduplex analysis detects frameshift and point mutations in patients with acute intermittent porphyria. Hum Genet 1995;96:161–6.
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عنوان ژورنال:
- Clinical chemistry
دوره 45 2 شماره
صفحات -
تاریخ انتشار 1999