Identification of two heterozygous deafness mutations in SLC26A4 (PDS) in a Chinese family with two siblings

J Chen, Q Wei, J Yao, X Qian, Y Dai… - … Journal of Audiology, 2013 - Taylor & Francis
Objective: To detect genetic cause of two Chinese siblings (patient 1 and 2) with Pendred
syndrome. Design: Patients and their parents underwent clinical and genetic evaluations. To …
被引用次数：9 相关文章

Identification of two heterozygous deafness mutations in SLC26A4 (PDS) in a Chinese family with two siblings

J Chen, Q Wei, J Yao, X Qian, Y Dai… - International …, 2013 - pubmed.ncbi.nlm.nih.gov
Objective To detect genetic cause of two Chinese siblings (patient 1 and 2) with Pendred
syndrome. Design Patients and their parents underwent clinical and genetic evaluations. To …