1. Bi-allelic mutations in MYL1 cause a severe congenital myopathy. (12th September 2018) Authors: Ravenscroft, Gianina; Zaharieva, Irina T; Bortolotti, Carlo A; Lambrughi, Matteo; Pignataro, Marcello; Borsari, Marco; Sewry, Caroline A; Phadke, Rahul; Haliloglu, Goknur; Ong, Royston; Goullée, Hayley; Whyte, Tamieka; Consortium, UK10K; Manzur, Adnan; Talim, Beril; Kaya, Ulkuhan; Osborn, Daniel ... Journal: Human molecular genetics Issue: Volume 27:Number 24(2018:Dec. 15) Page Start: 4263 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Bi-allelic mutations in MYL1 cause a severe congenital myopathy. (12th September 2018) Authors: Ravenscroft, Gianina; Zaharieva, Irina T; Bortolotti, Carlo A; Lambrughi, Matteo; Pignataro, Marcello; Borsari, Marco; Sewry, Caroline A; Phadke, Rahul; Haliloglu, Goknur; Ong, Royston; Goullée, Hayley; Whyte, Tamieka; Consortium, UK10K; Manzur, Adnan; Talim, Beril; Kaya, Ulkuhan; Osborn, Daniel ... Journal: Human molecular genetics Issue: Volume 27:Number 24(2018:Dec. 15) Page Start: 4263 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Label free urea biosensor based on organic electrochemical transistors. (14th June 2018) Authors: Berto, Marcello; Diacci, Chiara; Theuer, Lorenz; Di Lauro, Michele; Simon, Daniel T; Berggren, Magnus; Biscarini, Fabio; Beni, Valerio; Bortolotti, Carlo A Journal: Flexible and printed electronics Issue: Volume 3:Number 2(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗