1.
de Rooij FWM, Kavelaars FG, Koole-Lesuis H, Wilson JHP. Evidence for an ancestral founder of the common R116W mutation in the hydroxymethylbilane synthase gene in acute intermittent porphyria in the netherlands. Cell Mol Biol (Noisy-le-grand) [Internet]. 2009 Jul. 1 [cited 2024 Nov. 23];55(2):64-9. Available from: https://mail.cellmolbiol.org/index.php/CMB/article/view/1089