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Disease and Phenotype Relevant Genetic Variants Identified from Histone Acetylomes in Human Hearts
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The Mpdz KO mouse model characterized by my lab (Yang et al., EMBO Mol Med, 2019) phenocopies congenital hydrocephalus in patients harboring loss-of-function mutations in the human homologue, MPDZ…
Mollie Huber1, Denise Drotar2, Helmut Hiller3, Maria Beery3, Paul Joseph3, Irina Kusmartseva3 , Stephan Speier2 , Todd Brusko1, Maigan Brusko1, Mark Atkinson3 , Edward Phelps4, and Clayton Mathews1
INTEGRATION OF HUMAN GENETICS AND MUTLI-OMICS DATA IMPLICATES NOVEL PATHWAYS IN HYDROCEPHALUS
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