Stereocilin gene mutations associated with vertigo: Expansion of the DFNB16 phenotype

被引：0
|
作者：
Frykholm, C. A. [1 ]
Klar, J. [1 ,2 ]
Tomanovic, T. [3 ]
Ameur, A. [2 ]
Dahl, N. [1 ,2 ]
机构：
[1] Dept Immunol Genet & Pathol, Uppsala, Sweden
[2] Uppsala Univ, Biomed Ctr, Sci Life Lab, Uppsala, Sweden
[3] Karolinska Univ Hosp, Dept Hearing & Balance Disorders, Stockholm, Sweden
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2019年 / 27卷
基金：
瑞典研究理事会;
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P02.55B
引用
收藏
页码：69 / 69
页数：1
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