Update on enzyme and molecular defects in porphyria
Author:
Publisher
Wiley
Subject
Dermatology,Radiology, Nuclear Medicine and imaging,Immunology,General Medicine,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0781.1998.tb00014.x/fullpdf
Reference25 articles.
1. Porphobilinogen deaminase and uroporphyrinogen III synthase;Shoolingin-Jordan;J Bioenerg Biomembr,1995
2. Molecular epidemiology and diagnosis of PBG deaminase gene defects in acute intermittent porphyria;Puy;Am J Hum Genet,1997
3. Genetic defects in the porphyrias: types and significance;Elder;Clin Dermatol,1998
4. Hepatic porphyrias in children;Elder;J Inherit Metab Dis,1997
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