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2021 | 2 |
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A knock-in mouse model of Pendred syndrome with Slc26a4 L236P mutation.
Biochem Biophys Res Commun. 2019 Jul 23;515(2):359-365. doi: 10.1016/j.bbrc.2019.05.157. Epub 2019 May 30.
Biochem Biophys Res Commun. 2019.
PMID: 31155292
Insights into phenotypic differences between humans and mice with p.T721M and other C-terminal variants of the SLC26A4 gene.
Hu CJ, Lu YC, Tsai CY, Chan YH, Lin PH, Lee YS, Yu IS, Lin SW, Liu TC, Hsu CJ, Yang TH, Cheng YF, Wu CC.
Hu CJ, et al.
Sci Rep. 2021 Oct 25;11(1):20983. doi: 10.1038/s41598-021-00448-7.
Sci Rep. 2021.
PMID: 34697379
Free PMC article.
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Toward the Pathogenicity of the SLC26A4 p.C565Y Variant Using a Genetically Driven Mouse Model.
Hu CJ, Lu YC, Yang TH, Chan YH, Tsai CY, Yu IS, Lin SW, Liu TC, Cheng YF, Wu CC, Hsu CJ.
Hu CJ, et al.
Int J Mol Sci. 2021 Mar 10;22(6):2789. doi: 10.3390/ijms22062789.
Int J Mol Sci. 2021.
PMID: 33801843
Free PMC article.
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