DDX10 c.589A>G ;(p.T197A)

Variant ID: 11-108549093-A-G

NM_004398.2(DDX10):c.589A>G;(p.T197A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Desminopathy: Novel Desmin Variants, a New Cardiac Phenotype, and Further Evidence for Secondary Mitochondrial Dysfunction.

Journal Of Clinical Medicine
Kubánek, Miloš M; Schimerová, Tereza T; Piherová, Lenka L; Brodehl, Andreas A; Krebsová, Alice A; Ratnavadivel, Sandra S; Stanasiuk, Caroline C; Hansíková, Hana H; Zeman, Jiří J; Paleček, Tomáš T; Houštěk, Josef J; Drahota, Zdeněk Z; Nůsková, Hana H; Mikešová, Jana J; Zámečník, Josef J; Macek, Milan M; Ridzoň, Petr P; Malusková, Jana J; Stránecký, Viktor V; Melenovský, Vojtěch V; Milting, Hendrik H; Kmoch, Stanislav S
Publication Date: 2020-03-29

Variant appearance in text: DDX10: 589A>G
PubMed Link: 32235386
Variant Present in the following documents:
  • jcm-09-00937-s001.pdf
View BVdb publication page