DMD c.2614dup ;(p.I872Nfs*3)

Variant ID: X-32509401-A-AT

NM_004006.2(DMD):c.2614dup;(p.I872Nfs*3)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes.

Bmc Genetics
Bennett, Richard R RR; Schneider, Hal E HE; Estrella, Elicia E; Burgess, Stephanie S; Cheng, Andrew S AS; Barrett, Caitlin C; Lip, Va V; Lai, Poh San PS; Shen, Yiping Y; Wu, Bai-Lin BL; Darras, Basil T BT; Beggs, Alan H AH; Kunkel, Louis M LM
Publication Date: 2009-10-18

Variant appearance in text: DMD: 2614_2615insA
PubMed Link: 19835634
Variant Present in the following documents:
  • Main text
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