The E1784K mutation SCN5A is associated with mixed phenotype of type 3 long QT syndrome

Bibliographic Information

Title
The E1784K mutation SCN5A is associated with mixed phenotype of type 3 long QT syndrome
Author
Makita N, et. al.

Journal

Related Projects

See more

Details

  • CRID
    1010000781983946114
  • Article Type
    journal article
  • Data Source
    • KAKEN

Report a problem

Back to top