Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case report.
斯洛伐克家族中发现一种新的EYA4变异，导致晚发性常染色体显性遗传性听力损失：病例报告
期刊:BMC Medical Genetics
影响因子:
doi:10.1186/s12881-019-0806-y
Varga Lukas, Danis Daniel, Skopkova Martina, Masindova Ivica, Slobodova Zuzana, Demesova Lucia, Profant Milan, Gasperikova Daniela
