Association of SLC26A4 mutations, morphology, and hearing in pendred syndrome and NSEVA-Reference-Cited by-同舟云学术

Association of SLC26A4 mutations, morphology, and hearing in pendred syndrome and NSEVA

Author:

Mey Kristianna¹^ORCID,Muhamad Ali A.²,Tranebjærg Lisbeth³⁴,Rendtorff Nanna D.³,Rasmussen Stig H.⁵,Bille Michael¹,Cayé‐Thomasen Per¹⁶

Affiliation:

1. Department of OtorhinolaryngologyHead and Neck Surgery and Audiology Rigshospitalet/Gentofte Hellerup

2. the Department of Neuroradiology, Rigshospitalet

3. the Department of Clinical GeneticsRigshospitalet/The Kennedy Center

4. the Institute of Clinical Medicine

5. the Big Data Team, Municipality of Copenhagen

6. Faculty of Health and Medical SciencesUniversity of Copenhagen Copenhagen Denmark

Funder

Oticon Fonden

Publisher

Wiley

Subject

Otorhinolaryngology

Link

Reference46 articles.

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