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A novel deep intronic "SERPING1" variant as a cause of here..:
Vatsiou, Sofia
;
Zamanakou, Maria
;
Loules, Gedeon
...
Allergology International, T. 69, nr 3, s. 443-449. , 2020
Link:
https://ruj.uj.edu.pl/xmlui/handle/item/257077
RT Journal T1
A novel deep intronic "SERPING1" variant as a cause of hereditary angioedema due to C1-inhibitor deficiency
UL https://suche.suub.uni-bremen.de/peid=base-ftjagiellonuniir:oai:ruj.uj.edu.pl:item_257077&Exemplar=1&LAN=DE A1 Vatsiou, Sofia A1 Zamanakou, Maria A1 Loules, Gedeon A1 Psarros, Fotis A1 Parsopoulou, Faidra A1 Csuka, Dorottya A1 Valerieva, Anna A1 Staevska, Maria A1 Porębski, Grzegorz A1 Obtułowicz, Krystyna A1 Magerl, Markus A1 Maurer, Marcus A1 Speletas, Matthaios A1 Farkas, Henriette A1 Germenis, Anastasios E YR 2020 K1 C1-inhibitor deficiency K1 hereditary angioedema K1 intronic mutations K1 next-generation sequencing K1 SERPING1 gene JF Allergology International, T. 69, nr 3, s. 443-449 LK http://dx.doi.org/https://ruj.uj.edu.pl/xmlui/handle/item/257077 DO https://ruj.uj.edu.pl/xmlui/handle/item/257077 SF ELIB - SuUB Bremen
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