Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization

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Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization Empty Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization

Post  Jon Moulton on Mon May 06, 2013 9:50 am

Twigg SR, Lloyd D, Jenkins D, Elçioglu NE, Cooper CD, Al-Sannaa N, Annagür A, Gillessen-Kaesbach G, Hüning I, Knight SJ, Goodship JA, Keavney BD, Beales PL, Gileadi O, McGowan SJ, Wilkie AO. Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization. Am J Hum Genet. 2012 Nov 2;91(5):897-905. doi: 10.1016/j.ajhg.2012.08.027. Epub 2012 Oct 11.
Jon Moulton
Jon Moulton

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