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8. A novel heterozygous mutation in the HMBS gene in a patient with acute intermittent porphyria and posterior reversible encephalopathy syndrome. Yang Y; Chen X; Wu H; Peng H; Sun W; He B; Yuan Z Mol Med Rep; 2020 Jul; 22(1):516-524. PubMed ID: 32377710 [TBL] [Abstract][Full Text] [Related]
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15. Molecular study of the hydroxymethylbilane synthase gene (HMBS) among Polish patients with acute intermittent porphyria. Gregor A; Schneider-Yin X; Szlendak U; Wettstein A; Lipniacka A; Rüfenacht UB; Minder EI Hum Mutat; 2002 Mar; 19(3):310. PubMed ID: 11857754 [TBL] [Abstract][Full Text] [Related]
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