Genetics
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18 june 2020 11:22:50 |
| Further identification of a 140bp sequence from amid intron 9 of human FMR1 gene as a new exon (BMC Genetics) |
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Tweet 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... |
| 301 viewsCategory: Genetics |
 An IL17RA frameshift variant in a Holstein cattle family with psoriasis-like skin alterations and immunodeficiency (BMC Genetics)Design of experiments for fine-mapping quantitative trait loci in livestock populations (BMC Genetics) 
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