Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: PPOX[original query] |
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Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyria. Experimental dermatology 2005 1 14 (1): 50-5. de Villiers J Nico P, Kotze Maritha J, van Heerden Carel J, Sadie Annalene, Gardner Helena F J, Liebenberg Juanita, van Zyl René, du Plessis Lana, Kimberg Matti, Frank Jorge, Warnich Loui |
A next-generation-sequencing panel for mutational analysis of dominant acute hepatic porphyrias. Scandinavian journal of clinical and laboratory investigation 2019 6 79 (5): 305-313. Barman-Aksözen Jasmin, Suter Lukas, Wegmann Franziska, Meienberg Janine, Minder Anna Elisabeth, Beer Marc, Komminoth Paul, Minder Elisabeth I, Schneider-Yin Xiao |
Heterogeneous molecular behavior in liver tumors (HCC and CCA) of two patients with acute intermittent porphyria. Journal of cancer research and clinical oncology 2022 10 . Haverkamp Thomas, Bronisch Olivia, Knösel Thomas, Mogler Carolin, Weichert Wilko, Stauch Thomas, Schmid Claudia, Rummeny Claudia, Beykirch Maria K, Petrides Petro |
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- Page last updated:Apr 16, 2024
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