tryptophan and Optic Atrophy, Hereditary, Leber

tryptophan has been researched along with Optic Atrophy, Hereditary, Leber in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bulman, D; Damji, KF; Gupta, SK; Hussein, N; Jamal, A; Karim, N; Khan, R; Koenekoop, RK; Ladak, SS; Loyer, M; Rahim, M; Sohocki, MM	1

Other Studies

1 other study(ies) available for tryptophan and Optic Atrophy, Hereditary, Leber

Article	Year
Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p. Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, 2001, Volume: 36, Issue:5 Topics: Adaptor Proteins, Signal Transducing; Adolescent; Adult; Aged; Blindness; Carrier Proteins; Child; Child, Preschool; Chromosomes, Human, Pair 17; Codon, Nonsense; Codon, Terminator; Consanguinity; DNA Mutational Analysis; Eye Proteins; Female; Genetic Linkage; Haplotypes; Humans; Keratoconus; Male; Middle Aged; Optic Atrophy, Hereditary, Leber; Pakistan; Pedigree; Polymorphism, Genetic; Retinitis Pigmentosa; Tryptophan	2001

Article

Year

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

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, 2001, Volume: 36, Issue:5

Topics: Adaptor Proteins, Signal Transducing; Adolescent; Adult; Aged; Blindness; Carrier Proteins; Child; Child, Preschool; Chromosomes, Human, Pair 17; Codon, Nonsense; Codon, Terminator; Consanguinity; DNA Mutational Analysis; Eye Proteins; Female; Genetic Linkage; Haplotypes; Humans; Keratoconus; Male; Middle Aged; Optic Atrophy, Hereditary, Leber; Pakistan; Pedigree; Polymorphism, Genetic; Retinitis Pigmentosa; Tryptophan

2001