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14. A large deletion on chromosome 11 in acute intermittent porphyria. Di Pierro E; Besana V; Moriondo V; Brancaleoni V; Tavazzi D; Casalgrandi G; Ventura P; Rocchi E; Cappellini MD Blood Cells Mol Dis; 2006; 37(1):50-4. PubMed ID: 16828319 [TBL] [Abstract][Full Text] [Related]
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20. Novel HMBS founder mutation and significant intronic polymorphism in Spanish patients with acute intermittent porphyria. Guillén-Navarro E; Carbonell P; Glover G; Sánchez-Solís M; Fernández-Barreiro A Ann Hum Genet; 2004 Sep; 68(Pt 5):509-14. PubMed ID: 15469427 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]