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Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome.
Gerards M, Sluiter W, van den Bosch BJ, de Wit LE, Calis CM, Frentzen M, Akbari H, Schoonderwoerd K, Scholte HR, Jongbloed RJ, Hendrickx AT, de Coo IF, Smeets HJ. Gerards M, et al. Among authors: de wit le, de coo if. J Med Genet. 2010 Aug;47(8):507-12. doi: 10.1136/jmg.2009.067553. Epub 2009 Jun 18. J Med Genet. 2010. PMID: 19542079 Free PMC article.
Hormonal control of cardiac lipolysis by glyco(geno)lysis.
Hülsmann WC, De Wit LE, Stam H, Schoonderwoerd K. Hülsmann WC, et al. Among authors: de wit le. Biochim Biophys Acta. 1990 Nov 12;1055(2):189-92. doi: 10.1016/0167-4889(90)90121-s. Biochim Biophys Acta. 1990. PMID: 2146976
30 results