Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus-Reference-Cited by-同舟云学术

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Published:2006-10-01 Issue:11 Volume:38 Page:1242-1244
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Tarpey Patrick,Thomas Shery,Sarvananthan Nagini,Mallya Uma,Lisgo Steven,Talbot Chris J,Roberts Eryl O,Awan Musarat,Surendran Mylvaganam,McLean Rebecca J,Reinecke Robert D,Langmann Andrea,Lindner Susanne,Koch Martina,Jain Sunila,Woodruff Geoffrey,Gale Richard P,Bastawrous Andrew,Degg Chris,Droutsas Konstantinos,Asproudis Ioannis,Zubcov Alina A,Pieh Christina,Veal Colin D,Machado Rajiv D,Backhouse Oliver C,Baumber Laura,Constantinescu Cris S,Brodsky Michael C,Hunter David G,Hertle Richard W,Read Randy J,Edkins Sarah,O'Meara Sarah,Parker Adrian,Stevens Claire,Teague Jon,Wooster Richard,Futreal P Andrew,Trembath Richard C,Stratton Michael R,Raymond F Lucy,Gottlob Irene

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1893.pdf

Reference14 articles.

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3. Jacobs, J.B. & Dell'Osso, L.F. J. Vis. 4, 604–625 (2004).

4. Gottlob, I.Nystagmus. Curr. Opin. Ophthalmol. 12, 378–383 (2001).

5. Kerrison, J.B., Vagefi, M.R., Barmada, M.M. & Maumenee, I.H. Am. J. Hum. Genet. 64, 600–607 (1999).

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