APP c.1354C>G ;(p.Q452E)

Variant ID: 21-27347487-G-C

NM_000484.3(APP):c.1354C>G;(p.Q452E)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond.

The Journal Of Allergy And Clinical Immunology
Agostoni, Angelo A; Aygören-Pürsün, Emel E; Binkley, Karen E KE; Blanch, Alvaro A; Bork, Konrad K; Bouillet, Laurence L; Bucher, Christoph C; Castaldo, Anthony J AJ; Cicardi, Marco M; Davis, Alvin E AE; De Carolis, Caterina C; Drouet, Christian C; Duponchel, Christiane C; Farkas, Henriette H; Fáy, Kálmán K; Fekete, Béla B; Fischer, Bettina B; Fontana, Luigi L; Füst, George G; Giacomelli, Roberto R; Gröner, Albrecht A; Hack, C Erik CE; Harmat, George G; Jakenfelds, John J; Juers, Mathias M; Kalmár, Lajos L; Kaposi, Pál N PN; Karádi, István I; Kitzinger, Arianna A; Kollár, Tímea T; Kreuz, Wolfhart W; Lakatos, Peter P; Longhurst, Hilary J HJ; Lopez-Trascasa, Margarita M; Martinez-Saguer, Inmaculada I; Monnier, Nicole N; Nagy, István I; Németh, Eva E; Nielsen, Erik Waage EW; Nuijens, Jan H JH; O'grady, Caroline C; Pappalardo, Emanuela E; Penna, Vincenzo V; Perricone, Carlo C; Perricone, Roberto R; Rauch, Ursula U; Roche, Olga O; Rusicke, Eva E; Späth, Peter J PJ; Szendei, George G; Takács, Edit E; Tordai, Attila A; Truedsson, Lennart L; Varga, Lilian L; Visy, Beáta B; Williams, Kayla K; Zanichelli, Andrea A; Zingale, Lorenza L
Publication Date: 2004-09

Variant appearance in text: APP: Q452E
PubMed Link: 15356535
Variant Present in the following documents:
  • Main text
  • main.pdf
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