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Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p

✍ Scribed by Damji, Karim F.; Sohocki, Melanie M.; Khan, Ravesh; Gupta, Sanjoy K.; Rahim, Musa; Loyer, Magali; Hussein, Naushad; Karim, Nermin; Ladak, Shenif S.; Jamal, Alnoor; Bulman, Dennis; Koenekoop, Robert K.


Book ID
125824097
Publisher
Canadian Ophthalmological Society
Year
2001
Tongue
English
Weight
968 KB
Volume
36
Category
Article
ISSN
0008-4182

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