Article

Repression of ferritin light chain translation by human eIF3

2018-05-08

Abstract excerpt

A central problem in human biology remains the discovery of causal molecular links between mutations identified in genome-wide association studies (GWAS) and their corresponding disease traits. This challenge is magnified for variants residing in non-coding regions of the genome. Single-nucleotide polymorphisms (SNPs) in the 5’ untranslated region (5’-UTR) of the ferritin light chain ( FTL ) gene that cause hyper...

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Literature Corpus work: c6a50a94-8231-5809-b084-49fbac6e616f
DOI: 10.1101/316299

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