P24 Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signalling

✍ Scribed by Sharpe, J.A.; Logan, C.V.; Szabadkai, G.; Parry, D.A.; Torelli, S.; Childs, A.-M.; Kriek, M.; Phadke, R.; Johnson, C.A.; Roberts, N.Y.; Bonthron, D.T.; Pysden, K.A.; Whyte, T.; Munteanu, I.; Foley, A.R.; Wheway, G.; Szymanska, K.; Natarajan, S.; Abdelhamed, Z.A.; Morgan, J.E.; Roper, H.; Santen, G.W.E.; Niks, E.H.; van der Pol, W.L.; Lindhout, D.; Raffaello, A.; De Stefani, D.; den Dunnen, J.T.; Sun, Y.; Ginjaar, I.; Sewry, C.A.; Hurles, M.; Rizzuto, R.; Duchen, M.R.; Muntoni, F.; Sheridan, E.

• Book ID: 122325919
• Publisher: Elsevier Science
• Year: 2014
• Tongue: English
• Weight: 57 KB
• Volume: 24
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/S0960-8966(14)70040-9