Mutations in eight small DFNB genes are not a frequent cause of non-syndromic hereditary hearing loss in Czech patients
| Autor: | Marková, Simona *, Šafka Brožková, Dana, Mészárosová, Anna, Neupauerová, Jana, Groh, Daniel, Křečková, Gabriela, Laššuthová, Petra, Seeman, Pavel |
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| Zdroj: | In International Journal of Pediatric Otorhinolaryngology July 2016 86:27-33 |
| Databáze: | ScienceDirect |
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