Diagnostic Yield and Genetic Variation in 85 Swedish Patients with Mild to Profound Hearing Loss Analyzed by Whole Genome Sequencing
通过全基因组测序分析85名瑞典轻度至重度听力损失患者的诊断率和基因变异
期刊:Journal of Otolaryngology-Head & Neck Surgery
影响因子:2.2
doi:10.1177/19160216251345471
Elander, Johanna; Ullmark, Tove; Löwgren, Karolina; Stenfeldt, Karin; Falkenius-Schmidt, Karolina; Löfgren, Maria; Castiglione, Alessandro; Busi, Micol; Jonson, Tord; Ivarsson, Sofie; Ehrencrona, Hans; Ehinger, Johannes K; Värendh, Maria
