Article

Identification of microRNAs Associated With Human Fragile X Syndrome Using Next Generation Sequencing

2021-05-21

Abstract excerpt

Fragile X syndrome (FXS) is caused by a mutation in the FMR1 gene which can lead to a loss or shortage of the FMR1 protein. This protein interacts with specific miRNAs, and a change can cause a range of neurological disorders. Therefore, miRNAs could act as a novel class of potential biomarkers for common CNS diseases. The aim of this study was to test this theory by exploring the expression profiles of various mi...

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Literature Corpus work: 48a6fd07-1a02-5358-971f-cf8d97eb7c65
DOI: 10.21203/rs.3.rs-523429/v1

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