Connexin 26 (GJB2) mutations, causing KID Syndrome, are associated with cell death due to calcium gating deregulation

✍ Scribed by Alessandro Terrinoni; Andrea Codispoti; Valeria Serra; Biagio Didona; Ernesto Bruno; Robert Nisticò; Michela Giustizieri; Marco Alessandrini; Elena Campione; Gerry Melino

• Book ID: 116300058
• Publisher: Elsevier Science
• Year: 2010
• Tongue: English
• Weight: 589 KB
• Volume: 394
• Category: Article
• ISSN: 0006-291X
• DOI: 10.1016/j.bbrc.2010.03.073