Acute intermittent porphyria (AIP) is an autosomal dominant inherited disease of heme metabolism caused by mutations in the hydroxymethylbilane synthase gene. Diagnosing AIP during an acute attack using traditional biochemical markers is unproblematic, but it can be difficult to obtain a definite di
โฆ LIBER โฆ
Evaluation of mutation screening by heteroduplex analysis in acute intermittent porphyria: comparison with denaturing gradient gel electrophoresis
โ Scribed by D Tchernitchko; J Lamoril; H Puy; A.M Robreau; C Bogard; R Rosipal; L Gouya; J.C Deybach; Y Nordmann
- Book ID
- 117075822
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 487 KB
- Volume
- 279
- Category
- Article
- ISSN
- 0009-8981
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