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Oxford University Press

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Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination

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Drosophila model of Meier‐Gorlin syndrome based on the mutation in a conserved C‐Terminal domain of Orc6

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John Wiley & Sons Inc

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LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle

By Dialynas George   Flannery Kaitlin M.   Zirbel Luka N.   Nagy Peter L.   Mathews Katherine D.   Moore Steven A.   Wallrath Lori L.  

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Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type 1 patients

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