1. Hereditary haemochromatosis caused by homozygous HJV mutation evolved through paternal disomy. (12th February 2014) Authors: Neřoldová, M.; Fraňková, S.; Stránecký, V.; Honsová, E.; Lukšan, O.; Beneš, M.; Michalová, K.; Kmoch, S.; Jirsa, M. Journal: Clinical genetics Issue: Volume 87:Number 1(2015:Jan.) Page Start: 96 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Lymphocyte activation receptors: new structural paradigms in group V of C-type animal lectins. (26th October 2004) Authors: Pavlíček, J.; Kavan, D.; Pompach, P.; Novák, P.; Lukšan, O.; Bezouška, K. Journal: Biochemical Society transactions Issue: Volume 32:Number 6(2004) Page Start: 1124 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗