bibliographicCitation |
Gerards M, Sluiter W, van den Bosch BJC, de Wit LEA, Calis CMH, Frentzen M, Akbari H, Schoonderwoerd K, Scholte HR, Jongbloed RJ, Hendrickx ATM, de Coo IFM, Smeets HJM. Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome. Journal of Medical Genetics. 2009 Jun 18;47(8):507–12. doi: 10.1136/jmg.2009.067553. |