https://www.selleckchem.com/JAK.html
Here we report on the variation unique to the cpp mutation, i.e. single-nucleotide variants and insertions or deletions. Although the candidate region contains several genes of interest with regard to the cpp phenotype, only one cpp-linked variant was predicted to have a significant physiological effect by causing a frameshift mutation in ESRP2, which has a role in tissue-specific splicing during development. © 2020 The Authors. Animal Genetics published by John Wiley Sons Ltd on behalf of Stichting International Foundation for Animal Genetics
إعجاب
علق
شارك
