Records 1 - 2
| Mutational spectrum and clinical features of patients with ACTG1 mutations identified by massively parallel DNA sequencing.
The Annals of otology, rhinology, and laryngology 2015 May 124 Suppl 1 84S-93S.
Miyagawa Maiko, Nishio Shin-Ya, Ichinose Aya, Iwasaki Satoshi, Murata Takaaki, Kitajiri Shin-Ichiro, Usami Shin-Ic
| Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss.
Journal of translational medicine 2014 12 (1): 311.
Wei Qinjun, Zhu Hongmei, Qian Xuli, Chen Zhibin, Yao Jun, Lu Yajie, Cao Xin, Xing Guangqi