Absence of a trafficking defect in R1232W/T1620M, a double SCN5A mutant responsible for Brugada syndrome

Naomasa Makita, Naoki Mochizuki, Hiroyuki Tsutsui

Research output: Contribution to journalArticlepeer-review

18 Citations (Scopus)

Fingerprint

Dive into the research topics of 'Absence of a trafficking defect in R1232W/T1620M, a double SCN5A mutant responsible for Brugada syndrome'. Together they form a unique fingerprint.

Medicine and Dentistry

Neuroscience

Biochemistry, Genetics and Molecular Biology