Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p by Damji, Karim F., MD, Sohocki, Melanie M., PhD, Khan, Ravesh, MB BS, Gupta, Sanjoy K., MD, PhD, Rahim, Musa, MB BS, MHA, Loyer, Magali, MSc, Hussein, Naushad, MD, Karim, Nermin, OD, Ladak, Shenif S., MD, Jamal, Alnoor, MS, Bulman, Dennis, PhD, Koenekoop, Robert K., MD, PhD

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