A filter paper dry blood spot procedure for acute intermittent porphyria population screening by use of whole blood uroporphyrinogen-I-synthase assay

Author:

Johansson Lena,Thunell Stig,Wetterberg Lennart

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

Reference36 articles.

1. Intermittent acute prophyria — demonstration of genetic defect in porphobilinogen metabolism;Meyer;N Engl J Med,1972

2. Decreased red cell UPG-S activity in A1P;Strand;J Clin Invest,1972

3. A microassay for uroporphyrinogen-I-synthase, one of three abnormal enzyme activities in acute intermittent porphyria. and its application to the study of the genetics of this disease;Sassa,1974

4. Uroporphyrinogen-I-synthetase activity in the diagnosis of acute intermittent porphyria;Whitfield;Clin Chem,1975

5. Red cell uroporphyrinogen-I-synthetase in acute intermittent porphyria;Mustajoki;Ann Clin Res,1976

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