Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene. | Hum Mol Genet;31(3): 455-470, 2022 02 03. | MEDLINE

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Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene.

de Jong, Sarah; de Breuk, Anita; Volokhina, Elena B; Bakker, Bjorn; Garanto, Alejandro; Fauser, Sascha; Katti, Suresh; Hoyng, Carel B; Lechanteur, Yara T E; van den Heuvel, Lambert P; den Hollander, Anneke I.

Hum Mol Genet ; 31(3): 455-470, 2022 02 03.

Article in En | MEDLINE | ID: mdl-34508573

Subject(s)

Macular Degeneration; Polymorphism, Single Nucleotide; Aged; Complement Factor H/genetics; Complement System Proteins/genetics; Heterozygote; Humans; Macular Degeneration/genetics; Mutation, Missense

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Single Nucleotide / Macular Degeneration Limits: Aged / Humans Language: En Journal: Hum Mol Genet Year: 2022 Document type: Article

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Single Nucleotide / Macular Degeneration Limits: Aged / Humans Language: En Journal: Hum Mol Genet Year: 2022 Document type: Article