Article

Further identification of a 140bp sequence from amid intron 9 of human FMR1 gene as a new exon

2020-06-12

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> the disease gene of fragile X syndrome, <italic>FMR1</italic> gene, encodes fragile X mental retardation protein (FMRP). The alternative splicing (AS) of <italic>FMR1</italic> can affect the structure and function of FMRP. However, the biological functions of alternatively spliced isoforms remain elusive. In a previous study, we identified a new 140 bp exon from...

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Literature Corpus work: 0e226edc-6b1c-5189-8f11-ad93c13cc2ba
DOI: 10.21203/rs.2.20949/v3

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