Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss

G Yao, D Chen, H Wang, S Li, J Zhang… - Acta Oto …, 2013 - Taylor & Francis
Conclusions: This study demonstrated high prevalence of GJB2, SLC26A4, and mtDNA
A1555G mutations in Chinese patients with nonsyndromic hearing loss and discovered …
被引用次数：9 相关文章

[引用][C] Novel mutations ofSLC26A4in Chinese patients with nonsyndromic hearing loss

G Yao, D Chen, H Wang, S Li, J Zhang, Z Feng… - Acta Oto …, 2013 - cir.nii.ac.jp
Novel mutations of<i>SLC26A4</i>in Chinese patients with nonsyndromic hearing loss | CiNii
Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索フォームへ移動 …

Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss.

G Yao, D Chen, H Wang, S Li, J Zhang… - Acta Oto …, 2013 - search.ebscohost.com
Conclusions: This study demonstrated high prevalence of GJB2, SLC26A4, and mtDNA
A1555G mutations in Chinese patients with nonsyndromic hearing loss and discovered …

Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss

G Yao, D Chen, H Wang, S Li, J Zhang… - Acta oto …, 2013 - pubmed.ncbi.nlm.nih.gov
Conclusions This study demonstrated high prevalence of GJB2, SLC26A4, and mtDNA
A1555G mutations in Chinese patients with nonsyndromic hearing loss and discovered …

Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss.

G Yao, D Chen, H Wang, S Li, J Zhang… - Acta Oto …, 2013 - europepmc.org
Conclusions This study demonstrated high prevalence of GJB2, SLC26A4, and mtDNA
A1555G mutations in Chinese patients with nonsyndromic hearing loss and discovered …