PRRT2 c.1013-61C>T

Variant ID: 16-29825888-C-T

NM_145239.2(PRRT2):c.1013-61C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants.

Cells
Sutherland, Heidi G HG; Maksemous, Neven N; Albury, Cassie L CL; Ibrahim, Omar O; Smith, Robert A RA; Lea, Rod A RA; Haupt, Larisa M LM; Jenkins, Bronwyn B; Tsang, Benjamin B; Griffiths, Lyn R LR
Publication Date: 2020-10-28

Variant appearance in text: rs565298585
PubMed Link: 33126486
Variant Present in the following documents:
  • Main text
  • cells-09-02368.pdf
View BVdb publication page