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22-4
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Glaucoma Dialogue
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Author #41890
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Fan B
24
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Fan B
98388
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Collantes ERA
Human Mutation
2022; 43: 240-252
98535
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Simcoe MJ
Ophthalmology
2022; 129: 626-636
98388
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Delfin MS
Human Mutation
2022; 43: 240-252
98535
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Shah A; Fan B
Ophthalmology
2022; 129: 626-636
98388
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Fan B; Torregosa JMR
Human Mutation
2022; 43: 240-252
98535
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Choquet H
Ophthalmology
2022; 129: 626-636
98388
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Siguan-Bell C
Human Mutation
2022; 43: 240-252
98535
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Weisschuh N; Waseem NH
Ophthalmology
2022; 129: 626-636
98388
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Florcruz NVG
Human Mutation
2022; 43: 240-252
98535
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Jiang C
Ophthalmology
2022; 129: 626-636
98388
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Martinez JMD; Masna-Hidalgo BJ
Human Mutation
2022; 43: 240-252
98535
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Melles RB
Ophthalmology
2022; 129: 626-636
98388
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Guzman VPT
Human Mutation
2022; 43: 240-252
98535
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Ritch R
Ophthalmology
2022; 129: 626-636
98388
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Anotado-Flores JF
Human Mutation
2022; 43: 240-252
98535
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Mahroo OA; Wissinger B
Ophthalmology
2022; 129: 626-636
98388
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Levina FD; Hernandez SRC
Human Mutation
2022; 43: 240-252
98535
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Jorgenson E; Wiggs JL
Ophthalmology
2022; 129: 626-636
98388
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Collantes AA
Human Mutation
2022; 43: 240-252
98535
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Garway-Heath DF
Ophthalmology
2022; 129: 626-636
98388
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Sibulo MC; Rong S
Human Mutation
2022; 43: 240-252
98535
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Hysi PG
Ophthalmology
2022; 129: 626-636
98388
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Wiggs JL
Human Mutation
2022; 43: 240-252
98535
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Hammond CJ
Ophthalmology
2022; 129: 626-636
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