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American Journal of Ophthalmology
Volume 127, Issue 4
, Pages
426-435
, April 1999
Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14
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☆ Supported by the Elizabeth C. King Trust, the Ruben and Mollie Gordon Foundation, the Eye Research Institute, the Estates of Betty Gross, Margaret Mercer, and Martha W. S. Rogers, and an unrestricted grant from Research to Prevent Blindness, Inc, New York, New York, and Macular Degeneration International at the Wills Eye Hospital, Philadelphia, Pennsylvania. The Kyle Curran Fund, an unrestricted grant from Research to Prevent Blindness, Inc, the Foundation Fighting Blindness (Dr Weleber), and the Heed Ophthalmic Foundation (Dr Edwards) provided support at the Casey Eye Institute.
PII: S0002-9394(98)00331-6
© 1999 Elsevier Science Inc. All rights reserved.
« Previous
Next »
American Journal of Ophthalmology
Volume 127, Issue 4
, Pages
426-435
, April 1999
