Video Link: https://www.youtube.com/watch?v=HK-TyKKW-ok

Dennis Drayna and the discoveries in the genetics of stuttering
Whilst I was collating information on Drayna I uncovered many pubmed publications of his research. There is a considerable number of titles including: A role for inherited metabolic deficits in persistent developmental stuttering. (Kang C, Drayna D. Mol Genet Metab. 2012 Jul 28.) Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q. (Raza MH, Amjad R, Riazuddin S, Drayna D. Hum Genet. 2012 Feb) Analysis of mannose 6-phosphate uncovering enzyme mutations associated with persistent stuttering. (Lee WS, Kang C, Drayna D, Kornfeld S. J Biol Chem. 2011 Nov) Evaluation of the association between polymorphisms at the DRD2 locus and stuttering. (Kang C, Domingues BS, Sainz E, Domingues CE, Drayna D, Moretti-Ferreira D. J Hum Genet. 2011 Jun) Characterization of a mutation commonly associated with persistent stuttering: evidence for a founder mutation. (Fedyna A, Drayna D, Kang C. J Hum Genet. 2011 Jan) Genomewide significant linkage to stuttering on chromosome 12. (Riaz N, Steinberg S, Ahmad J, Pluzhnikov A, Riazuddin S, Cox NJ, Drayna D. Am J Hum Genet. 2005 Apr) A model system for identifying genes underlying complex traits. Drayna D, Kim UK, Coon H, Jorgenson E, Risch N, Leppert M. Cold Spring Harb Symp Quant Biol. 2003 Results of a genome-wide linkage scan for stuttering. Shugart YY, Mundorff J, Kilshaw J, Doheny K, Doan B, Wanyee J, Green ED, Drayna D. Am J Med Genet A. 2004 Jan Link to pubmed: http://www.ncbi.nlm.nih.gov

By: lololcopter123

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Dennis Drayna and the discoveries in the genetics of stuttering - Video

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