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

Abstract Background The disease gene of fragile X syndrome, FMR1 gene, encodes fragile X mental retardation protein (FMRP). The alternative splicing (AS) of FMR1 can affect the structure and function of FMRP. However, the biological functions of alternatively spliced isoforms remain elusive. In a pr...

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Autors principals:	Wen-jing Yang, Ai-zhen Yan, Yong-jun Xu, Xiao-yan Guo, Xian-guo Fu, Dan Li, Juan Liao, Duo Zhang, Feng-hua Lan
Format:	Artigo
Idioma:	Inglês
Publicat:	BMC 2020-06-01
Col·lecció:	BMC Genetics
Matèries:	FMR1 FMRP FXS Alternative splicing Alternative exon
Accés en línia:	http://link.springer.com/article/10.1186/s12863-020-00870-2
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