C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy-Reference-Cited by-同舟云学术

C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

Published:2007-07-29 Issue:9 Volume:39 Page:1068-1070
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

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,Atkinson John P

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng2082.pdf

Reference15 articles.

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2. Grand, M.G. et al. Ophthalmology 95, 649–659 (1988).

3. Storimans, C.W. et al. Eur. J. Ophthalmol. 1, 73–78 (1991).

4. Terwindt, G.M. et al. Brain 121, 303–316 (1998).

5. Jen, J. et al. Neurology 49, 1322–1330 (1997).

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