HUJOVÁ, Pavla, Lucie GRODECKÁ, Přemysl SOUČEK, Hana GROMBIŘÍKOVÁ, Barbora RAVČUKOVÁ, Pavel KUKLÍNEK, Roman HAKL and Tomáš FREIBERGER. A new deep intronic mutation caused aberrant splicing in a family diagnosed with hereditary angioedema. In RNA and Diseases conference, Uppsala, Švédsko. 2018.
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Basic information
Original name A new deep intronic mutation caused aberrant splicing in a family diagnosed with hereditary angioedema
Authors HUJOVÁ, Pavla, Lucie GRODECKÁ, Přemysl SOUČEK, Hana GROMBIŘÍKOVÁ, Barbora RAVČUKOVÁ, Pavel KUKLÍNEK, Roman HAKL and Tomáš FREIBERGER.
Edition RNA and Diseases conference, Uppsala, Švédsko, 2018.
Other information
Type of outcome Requested lectures
Confidentiality degree is not subject to a state or trade secret
Organization unit Central European Institute of Technology
Changed by Changed by: Bc. Kateřina Kolesová, učo 112275. Changed: 27/12/2018 08:47.
Links
692298, interní kód MUName: MEDGENET - Medical genomics and epigenomics network (Acronym: MEDGENET)
Investor: European Union, Spreading excellence and widening participation
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