AKAP13 c.-11-30200T>C

Variant ID: 15-85998741-T-C

NM_007200.4(AKAP13):c.-11-30200T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Structural genomic variation in ischemic stroke.

Neurogenetics
Matarin, Mar M; Simon-Sanchez, Javier J; Fung, Hon-Chung HC; Scholz, Sonja S; Gibbs, J Raphael JR; Hernandez, Dena G DG; Crews, Cynthia C; Britton, Angela A; De Vrieze, Fabienne Wavrant FW; Brott, Thomas G TG; Brown, Robert D RD; Worrall, Bradford B BB; Silliman, Scott S; Case, L Douglas LD; Hardy, John A JA; Rich, Stephen S SS; Meschia, James F JF; Singleton, Andrew B AB
Publication Date: 2008-05

Variant appearance in text: rs12443473
PubMed Link: 18288507
Variant Present in the following documents:
  • Main text
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