DMD c.5524_5526delinsTGG ;(p.R1842W)

Variant ID: X-32364120-TCT-CCA

NM_004006.2(DMD):c.5524_5526delinsTGG;(p.R1842W)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent.

Frontiers In Neurology
Chakravorty, Samya S; Nallamilli, Babi Ramesh Reddy BRR; Khadilkar, Satish Vasant SV; Singla, Madhu Bala MB; Bhutada, Ashish A; Dastur, Rashna R; Gaitonde, Pradnya Satish PS; Rufibach, Laura E LE; Gloster, Logan L; Hegde, Madhuri M
Publication Date: 2020

Variant appearance in text: DMD: R1842W
PubMed Link: 33250842
Variant Present in the following documents:
  • Main text
  • fneur-11-559327.pdf
View BVdb publication page