The PDS Gene, Pendred Syndrome and Non-Syndromic Deafness (DFNB4)
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KARGER
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene;International Journal of Dermatology;2019-04-25
2. Two missense mutations in SLC26A4 gene: a molecular and functional study;Clinical Genetics;2009-12-02
3. Chromosome imbalances in syndromic hearing loss;Clinical Genetics;2009-11
4. Genética molecular da deficiência auditiva não-sindrômica;Revista Brasileira de Otorrinolaringologia;2005-04
5. Molecular genetics of non-syndromic deafness;Brazilian Journal of Otorhinolaryngology;2005-03
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