Open AccessVision 1 Year after Gene Therapy for Leber's Congenital Amaurosis
Author(s) -
Artur V. Cideciyan,
William W. Hauswirth,
Tomas S. Alemán,
Shalesh Kaushal,
Sharon Schwartz,
Sanford L. Boye,
Elizabeth A. M. Windsor,
Thomas J. Conlon,
Alexander Sumaroka,
Alejandro J. Román,
Barry J. Byrne,
Samuel G. Jacobson
Publication year - 2009
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmc0903652
Subject(s) - medicine , genetic enhancement , ophthalmology , amaurosis , optometry , gene , pediatrics , genetics , biology
To the Editor: Leber's congenital amaurosis, a common cause of blindness in infants and children,1 recently became the first human genetic retinal disease to show improved vision in response to tre...
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