TTN c.59352dup ;(p.E19785*)

Variant ID: 2-179457379-C-CA

NM_001267550.1(TTN):c.59352dup;(p.E19785*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Minoche, Andre E AE; Horvat, Claire C; Johnson, Renee R; Gayevskiy, Velimir V; Morton, Sarah U SU; Drew, Alexander P AP; Woo, Kerhan K; Statham, Aaron L AL; Lundie, Ben B; Bagnall, Richard D RD; Ingles, Jodie J; Semsarian, Christopher C; Seidman, J G JG; Seidman, Christine E CE; Dinger, Marcel E ME; Cowley, Mark J MJ; Fatkin, Diane D
Publication Date: 2019-03

Variant appearance in text: N/A
PubMed Link: 29961767
Variant Present in the following documents:
View BVdb publication page