DMD c.6438+86592G>A

Variant ID: X-32148441-C-T

NM_004006.2(DMD):c.6438+86592G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The possible role of chromosome X variability in hypertensive familiarity.

Journal Of Human Hypertension
Ciccarelli, M M; Finelli, R R; Rivera, N N; Santulli, G G; Izzo, R R; De Luca, N N; Rozza, F F; Ceccarelli, M M; Pagnotta, S S; Uliano, F F; Tremigliozzi, R R; Condorelli, G G; Trimarco, V V; Iaccarino, G G
Publication Date: 2017-01

Variant appearance in text: rs1317098
PubMed Link: 26911533
Variant Present in the following documents:
  • Main text
  • jhh20169a.pdf
View BVdb publication page