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. 2017 Jan 5;8(1):e2537. doi: 10.1038/cddis.2016.453

Table 1. Genotyping and clinical information of AMD and control RPE.

Donor Id# Donor age (gender) Clinical diagnosis CFH (C: risk) HTRA1 (A: risk) LOC (T: risk) Factor B (T: protective) C2 (C: protective) Smoking Cause of death Enucleation (h)
006 72 (M) CONTROL CT AG GT CC GG Quit in 1993 Chronic obstructive pulmonary disease 12
010 80 (M) CONTROL CC AG GT CC GG Quit in 1984 Acute myocardial infraction 9.4
015 11 (M) CONTROL TT AG GT CC GG No Multiple trauma 9.5
023 17 (M) CONTROL CT GG GG CT GG N/D Motor vehicle accident 9
025 50 (M) CONTROL TT GG GG CC GG No Myocardial infraction 17
009 68 (F) AMD TT GG GG TT GG 2 ppd for 40 years Stroke 3
014 82 (M) AMD CT AG GT CC GG 1 ppd for 40 years Cardial related 12
017 81 (M) AMD CC AA TT CC GG N/D Cardial arrest 10.5
019 80 (F) AMD CT GG GG CC GG No GI bleed 9
032 75 (F) AMD CT AA TT CC GG No Pancreatic cancer 7

Abbreviations: F, female; M, male

The five clinically diagnosed AMD donors and five clinically normal donors (control) from which primary RPE cultures were established. The cause of death and time of enucleation are indicated. Genotyping data for known AMD-associated Single Nuclear Polymorphisms showing the haplotypes of each donor, carrying risk or protective alleles as marked in bold entries

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