A rare penetrant mutation in CFH confers high risk of age-related macular degeneration

S Raychaudhuri, O Iartchouk, K Chin, PL Tan, AK Tai… - Nature …, 2011 - nature.com
Two common variants in the gene encoding complement factor H (CFH), the Y402H
substitution (rs1061170, c. 1204C> T),,, and the intronic rs1410996 SNP,, explain 17% of …
被引用次数：364 相关文章
[HTML] nih.gov

[HTML][HTML] A rare penetrant mutation in CFH confers high risk of age-related macular degeneration

S Raychaudhuri, O Iartchouk, K Chin, PL Tan… - Nature …, 2011 - ncbi.nlm.nih.gov
Two common variants within CFH, the Y402H 1–4 and the rs1410996 SNPs 5, 6, explain
17% of age-related macular degeneration (AMD) liability. However, proof for the …

A rare penetrant mutation in CFH confers high risk of age-related macular degeneration

S Raychaudhuri, O Iartchouk, K Chin… - Nature …, 2011 - pubmed.ncbi.nlm.nih.gov
Two common variants in the gene encoding complement factor H (CFH), the Y402H
substitution (rs1061170, c. 1204C> T)(1-4) and the intronic rs1410996 SNP (5, 6), explain …

A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.

S Raychaudhuri, O Iartchouk, K Chin, PL Tan… - Nature …, 2011 - search.ebscohost.com
Two common variants in the gene encoding complement factor H (CFH), the Y402H
substitution (rs1061170, c. 1204C> T) and the intronic rs1410996 SNP, explain 17% of …

A rare penetrant mutation in CFH confers high risk of age-related macular degeneration

S Raychaudhuri, O Iartchouk, K Chin… - Nature …, 2011 - scholars.northwestern.edu
Two common variants in the gene encoding complement factor H (CFH), the Y402H
substitution (rs1061170, c. 1204C> T) and the intronic rs1410996 SNP, explain 17% of age …

[引用][C] A rare penetrant mutation in CFH confers high risk of age-related macular degeneration

S RAYCHAUDHURI, O IARTCHOUK… - Nature …, 2011 - pascal-francis.inist.fr
A rare penetrant mutation in CFH confers high risk of age-related macular degeneration CNRS
Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple search …

A rare penetrant mutation in CFH confers high risk of age-related macular degeneration

S Raychaudhuri, O Iartchouk, K Chin, PL Tan, AK Tai… - Nature …, 2011 - go.gale.com
Two common variants in the gene encoding complement factor H (CFH), the Y402H
substitution (rs1061170, c. 1204C> T)(1-4) and the intronic rs1410996 SNP (5, 6), explain …
[PDF] psu.edu

[PDF][PDF] A rare penetrant mutation in CFH confers high risk of age-related macular degeneration

S Raychaudhuri, O Iartchouk, K Chin, PL Tan, A Tai… - Nat Genet - Citeseer
Two common variants within CFH, the Y402H1–4 and the rs1410996 SNPs5, 6, explain
17% of age-related macular degeneration (AMD) liability. However, proof for the …

A rare penetrant mutation in CFH confers high risk of age-related macular degeneration

S Raychaudhuri, O Iartchouk, K Chin, PL Tan… - Nature …, 2011 - pure.johnshopkins.edu
Two common variants in the gene encoding complement factor H (CFH), the Y402H
substitution (rs1061170, c. 1204C> T) and the intronic rs1410996 SNP, explain 17% of age …
[PDF] academia.edu

[PDF][PDF] A rare penetrant mutation in CFH confers high risk of age-related macular degeneration

S Raychaudhuri, O Iartchouk, K Chin, PL Tan, A Tai… - Nat Genet - academia.edu
Two common variants within CFH, the Y402H1–4 and the rs1410996 SNPs5, 6, explain
17% of age-related macular degeneration (AMD) liability. However, proof for the …