Identification of Disease-Causing Mutations in Autosomal Dominant Retinitis Pigmentosa (adRP) Using Next-Generation DNA Sequencing-Reference-Cited by-同舟云学术

Identification of Disease-Causing Mutations in Autosomal Dominant Retinitis Pigmentosa (adRP) Using Next-Generation DNA Sequencing

Published:2011-01-25 Issue:1 Volume:52 Page:494
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Bowne Sara J.¹,Sullivan Lori S.¹,Koboldt Daniel C.²,Ding Li²,Fulton Robert²,Abbott Rachel M.²,Sodergren Erica J.²,Birch David G.³,Wheaton Dianna H.³,Heckenlively John R.⁴,Liu Qin⁵,Pierce Eric A.⁵,Weinstock George M.²,Daiger Stephen P.¹

Affiliation:

1. From the Human Genetics Center, The University of Texas Health Science Center, Houston, Texas;

2. the Genome Sequencing Center, Washington University, St. Louis, Missouri;

3. the Retina Foundation of the Southwest, Dallas, Texas;

4. the Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan; and

5. the F. M. Kirby Center for Molecular Ophthalmology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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