DMD c.9139_9140insA ;(p.P3047Hfs*51)

Variant ID: X-31366696-G-GT

NM_004006.2(DMD):c.9139_9140insA;(p.P3047Hfs*51)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mutation analysis in a population-based cohort of boys with Duchenne or Becker muscular dystrophy.

Journal Of Child Neurology
Cunniff, Christopher C; Andrews, Jennifer J; Meaney, F John FJ; Mathews, Katherine D KD; Matthews, Dennis D; Ciafaloni, Emma E; Miller, Timothy M TM; Bodensteiner, John B JB; Miller, Lisa A LA; James, Katherine A KA; Druschel, Charlotte M CM; Romitti, Paul A PA; Pandya, Shree S
Publication Date: 2009-04

Variant appearance in text: DMD: 9139insA
PubMed Link: 19074751
Variant Present in the following documents:
  • Main text
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