DMD c.6906G>A ;(p.W2302*)

Variant ID: X-31947719-C-T

NM_004006.2(DMD):c.6906G>A;(p.W2302*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Efficient precise in vivo base editing in adult dystrophic mice.

Nature Communications
Xu, Li L; Zhang, Chen C; Li, Haiwen H; Wang, Peipei P; Gao, Yandi Y; Mokadam, Nahush A NA; Ma, Jianjie J; Arnold, W David WD; Han, Renzhi R
Publication Date: 2021-06-17

Variant appearance in text: DMD: 6906G>A
PubMed Link: 34140489
Variant Present in the following documents:
  • 41467_2021_23996_MOESM1_ESM.pdf
View BVdb publication page



Clinical and genetic characterization of manifesting carriers of DMD mutations.

Neuromuscular Disorders : Nmd
Soltanzadeh, Payam P; Friez, Michael J MJ; Dunn, Diane D; von Niederhausern, Andrew A; Gurvich, Olga L OL; Swoboda, Kathryn J KJ; Sampson, Jacinda B JB; Pestronk, Alan A; Connolly, Anne M AM; Florence, Julaine M JM; Finkel, Richard S RS; Bönnemann, Carsten G CG; Medne, Livija L; Mendell, Jerry R JR; Mathews, Katherine D KD; Wong, Brenda L BL; Sussman, Michael D MD; Zonana, Jonathan J; Kovak, Karen K; Gospe, Sidney M SM; Gappmaier, Eduard E; Taylor, Laura E LE; Howard, Michael T MT; Weiss, Robert B RB; Flanigan, Kevin M KM
Publication Date: 2010-08

Variant appearance in text: DMD: 6906G>A; Trp2302X
PubMed Link: 20630757
Variant Present in the following documents:
  • Main text
View BVdb publication page