Smim9-KO 基因敲除小鼠

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2. Jourdy, Yohann, Bardel, Claire, Fretigny, Mathilde, Vinciguerra, Christine, Schluth-Bolard, Caroline. 2021. Complete characterisation of two new large Xq28 duplications involving F8 using whole genome sequencing in patients without haemophilia A. In Haemophilia : the official journal of the World Federation of Hemophilia, 28, 117-124. doi:10.1111/hae.14402. https://pubmed.ncbi.nlm.nih.gov/34480810/

3. Abelleyro, Miguel Martín, Radic, Claudia Pamela, Marchione, Vanina Daniela, Rossetti, Liliana Carmen, De Brasi, Carlos Daniel. 2020. Molecular insights into the mechanism of nonrecurrent F8 structural variants: Full breakpoint characterization and bioinformatics of DNA elements implicated in the upmost severe phenotype in hemophilia A. In Human mutation, 41, 825-836. doi:10.1002/humu.23977. https://pubmed.ncbi.nlm.nih.gov/31898853/