A new deep intronic mutation caused aberrant splicing in a family diagnosed with hereditary angioedema

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Authors	HUJOVÁ Pavla GRODECKÁ Lucie SOUČEK Přemysl GROMBIŘÍKOVÁ Hana RAVČUKOVÁ Barbora KUKLÍNEK Pavel HAKL Roman FREIBERGER Tomáš
Year of publication	2018
MU Faculty or unit	Central European Institute of Technology
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Related projects:	MEDGENET - Medical genomics and epigenomics network