Associated Papers
Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations.
Yu X et al.
Orphanet Journal of Rare Diseases, 2020
31992338 (PubMed )
Supplement: 13023_2020_1311_MOESM1_ESM.docx
[The prenatal diagnosis and early intervention of nonsyndromic hearing loss of connexin26 gene].
He C et al.
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology, 2006
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