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Hearing Impairment with Monoallelic GJB2 Variants: A GJB2 Cause or Non-GJB2 Cause?
J Mol Diagn. 2021 Oct;23(10):1279-1291. doi: 10.1016/j.jmoldx.2021.07.007. Epub 2021 Jul 27.
J Mol Diagn. 2021.
PMID: 34325055
Free article.
Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese Population.
Wu CC, Tsai CY, Lin YH, Chen PY, Lin PH, Cheng YF, Wu CM, Lin YH, Lee CY, Erdenechuluun J, Liu TC, Chen PL, Hsu CJ.
Wu CC, et al. Among authors: erdenechuluun j.
Genes (Basel). 2019 Oct 1;10(10):772. doi: 10.3390/genes10100772.
Genes (Basel). 2019.
PMID: 31581539
Free PMC article.
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Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations.
Erdenechuluun J, Lin YH, Ganbat K, Bataakhuu D, Makhbal Z, Tsai CY, Lin YH, Chan YH, Hsu CJ, Hsu WC, Chen PL, Wu CC.
Erdenechuluun J, et al.
PLoS One. 2018 Dec 21;13(12):e0209797. doi: 10.1371/journal.pone.0209797. eCollection 2018.
PLoS One. 2018.
PMID: 30576380
Free PMC article.
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