Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p
- 1 August 2001
- journal article
- Published by Elsevier in Canadian Journal of Ophthalmology
- Vol. 36 (5) , 252-259
- https://doi.org/10.1016/s0008-4182(01)80018-1
Abstract
No abstract availableKeywords
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