Hematologically Important Mutations: Acute Intermittent Porphyria
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference65 articles.
1. The porphyrias;Kappas,1995
2. Acute intermittent porphyria;Grandchamp;Semin. Liv. Dis.,1998
3. The human gene mutation database;Cooper;Nucleic Acids Res.,1998
4. Non-erythroid form of acute intermittent porphyria caused by promoter and frameshift mutations distant from the coding sequence of exon 1 of the HMBS gene;Whatley;Hum. Genet.,2000
5. Acute intermittent porphyria: identification and expression of exonic mutations in the hydroxymethylbilane synthase gene. An initiation codon missense mutation in the housekeeping transcript causes "variant acute intermittent porphyria" with normal expression of the erythroid-specific enzyme.
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1. Network analysis of hydroxymethylbilane synthase dynamics;Journal of Molecular Graphics and Modelling;2020-09
2. Acute Intermittent Porphyria in Argentina: An Update;BioMed Research International;2015
3. The acute porphyrias: a diagnostic and therapeutic challenge in internal and emergency medicine;Internal and Emergency Medicine;2009-05-29
4. A novel 3-base deletion (IVS3+2_4delTGG) of the hydroxymethylbilane synthase gene in a Brazilian patient with acute intermittent porphyria;Genetics and Molecular Biology;2007
5. A large deletion on chromosome 11 in acute intermittent porphyria;Blood Cells, Molecules, and Diseases;2006-07
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