Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p. (Q34090525)
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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
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English | Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p. |
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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. (English)
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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 (English)
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K F Damji
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M M Sohocki
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R Khan
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S K Gupta
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M Rahim
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M Loyer
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N Hussein
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N Karim
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S S Ladak
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A Jamal
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D Bulman
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R K Koenekoop
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1 August 2001
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August 2001
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36
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252-259
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