DMD c.3786+2T>A

Variant ID: X-32466571-A-T

NM_004006.2(DMD):c.3786+2T>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Haplotype-Based Noninvasive Prenatal Diagnosis of 21 Families With Duchenne Muscular Dystrophy: Real-World Clinical Data in China.

Frontiers In Genetics
Kong, Lingrong L; Li, Shaojun S; Zhao, Zhenhua Z; Feng, Jun J; Chen, Guangquan G; Liu, Lina L; Tang, Weiqin W; Li, Suqing S; Li, Feifei F; Han, Xiujuan X; Wu, Di D; Zhang, Haichuan H; Sun, Luming L; Kong, Xiangdong X
Publication Date: 2021

Variant appearance in text: DMD: 3786+2T>A
PubMed Link: 34970304
Variant Present in the following documents:
  • Main text
  • fgene-12-791856.pdf
View BVdb publication page