USH2A c.9958+4171T>C

Variant ID: 1-215968078-A-G

NM_206933.2(USH2A):c.9958+4171T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and hereditary haemorrhagic telangiectasia.

Nature Communications
Benzinou, Michael M; Clermont, Frederic F FF; Letteboer, Tom G W TG; Kim, Jai-Hyun JH; Espejel, Silvia S; Harradine, Kelly A KA; Arbelaez, Juan J; Luu, Minh Thu MT; Roy, Ritu R; Quigley, David D; Higgins, Mamie Nakayama MN; Zaid, Musa M; Aouizerat, Bradley E BE; van Amstel, Johannes Kristian Ploos JK; Giraud, Sophie S; Dupuis-Girod, Sophie S; Lesca, Gaetan G; Plauchu, Henri H; Hughes, Christopher C W CC; Westermann, Cornelius J J CJ; Akhurst, Rosemary J RJ
Publication Date: 2012-01-10

Variant appearance in text: rs10746458
PubMed Link: 22233626
Variant Present in the following documents:
  • Main text
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