Related Articles
A clinical and multi‑omics study of Van der Woude syndrome in three generations of a Chinese family
A novel <em>KCNQ4</em> gene variant (c.857A>G; p.Tyr286Cys) in an extended family with non‑syndromic deafness 2A
Mutant GNAQ promotes cell viability and migration of uveal melanoma cells through the activation of Notch signaling
G protein subunit α q regulates gastric cancer growth via the p53/p21 and MEK/ERK pathways
Whole‑exome sequencing identifies a novel mutation (R367G) in SCN5A to be associated with familial cardiac conduction disease