Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene

被引：0
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作者：
Zdeněk Čada
Dana Šafka Brožková
Zuzana Balatková
Pavlína Plevová
Dagmar Rašková
Jana Laštůvková
Rudolf Černý
Veronika Bandúrová
Vladimír Koucký
Silvie Hrubá
Martin Komarc
Ján Jenčík
Simona Poisson Marková
Jan Plzák
Jan Kluh
Pavel Seeman
机构：
[1] Postgraduate Medical School,Department of Otorhinolaryngology and Head and Neck Surgery, 1st Faculty of Medicine, Charles University, Faculty Hospital Motol
[2] Charles University and Motol University Hospital,DNA Laboratory, Department of Paediatric Neurology, 2nd Faculty of Medicine
[3] Charles University and Motol University Hospital,Department of Neurology, 2nd Faculty of Medicine
[4] Charles University,Department of Anthropomotorics and Methodology, Faculty of Physical Education and Sport
[5] University Hospital Ostrava,Department of Medical Genetics
[6] Centre for Medical Genetics and Reproductive Medicine,Department of Medical Genetics
[7] Gennet,undefined
[8] Masaryk Hospital,undefined
[9] Regional Health Corporation,undefined
来源：
European Archives of Oto-Rhino-Laryngology | 2019年 / 276卷
关键词：
Autosomal recessive nonsyndromic hearing loss; DFNB16; STRC; Stereocilin; Audiological phenotype; Genotype/phenotype correlation;
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页码：3353 / 3358
页数：5
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