C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
Atkinson, John P, Richards, Anna, van den Maagdenberg, Arn M J M, Jen, Joanna C, Kavanagh, David, Bertram, Paula, Spitzer, Dirk, Liszewski, M Kathryn, Barilla-LaBarca, Maria-Louise, Terwindt, Gisela M, Kasai, Yumi, McLellan, Mike, Grand, Mark Gilbert, Vanmolkot, Kaate R J, de Vries, Boukje, Wan, Jijun, Kane, Michael J, Mamsa, Hafsa, Schäfer, Ruth, Stam, Anine H, Haan, Joost, de Jong, Paulus T V M, Storimans, Caroline W, van Schooneveld, Mary J, Oosterhuis, Jendo A, Gschwendter, Andreas, Dichgans, Martin, Kotschet, Katya E, Hodgkinson, Suzanne, Hardy, Todd A, Delatycki, Martin B, Hajj-Ali, Rula A, Kothari, Parul H, Nelson, Stanley F, Frants, Rune R, Baloh, Robert W, Ferrari, Michel D
Published in Nature genetics (01.09.2007)
Published in Nature genetics (01.09.2007)
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