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

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 previous s...

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Detalles Bibliográficos
Autores principales: Yang, Wen-jing, Yan, Ai-zhen, Xu, Yong-jun, Guo, Xiao-yan, Fu, Xian-guo, Li, Dan, Liao, Juan, Zhang, Duo, Lan, Feng-hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7301526/
https://www.ncbi.nlm.nih.gov/pubmed/32552710
http://dx.doi.org/10.1186/s12863-020-00870-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7301526/
https://www.ncbi.nlm.nih.gov/pubmed/32552710
http://dx.doi.org/10.1186/s12863-020-00870-2

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