DMD c.697_698delinsCA ;(p.T233Q)

Variant ID: X-32717362-GT-TG

NM_004006.2(DMD):c.697_698delinsCA;(p.T233Q)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: DMD: T233Q
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Development of Patient-specific AAV Vectors After Neutralizing Antibody Selection for Enhanced Muscle Gene Transfer.

Molecular Therapy : The Journal Of The American Society Of Gene Therapy
Li, Chengwen C; Wu, Shuqing S; Albright, Blake B; Hirsch, Matthew M; Li, Wuping W; Tseng, Yu-Shan YS; Agbandje-McKenna, Mavis M; McPhee, Scott S; Asokan, Aravind A; Samulski, R Jude RJ
Publication Date: 2016-02

Variant appearance in text: DMD: T233Q
PubMed Link: 26220272
Variant Present in the following documents:
  • Main text
View BVdb publication page