Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss.
Miyajima H, Moteki H, Day T, Nishio SY, Murata T, Ikezono T, Takeda H, Abe S, Iwasaki S, Takahashi M, Naito Y, Yamazaki H, Kanda Y, Kitajiri SI, Usami SI.
Miyajima H, et al. Among authors: moteki h.
Sci Rep. 2020 Apr 27;10(1):7056. doi: 10.1038/s41598-020-63690-5.
Sci Rep. 2020.
PMID: 32341388
Free PMC article.