# STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/strc-deletion-is-a-frequent-cause-of-slight-to-moderate-congenital-hearing/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Pavlína Plevová,Martina Paprskarova,Petra Tvrda,Petra Turska,Rastislav Slavkovský,Eva Mrázková |
| Citations | 33 |
| DOI | 10.1097/mao.0000000000001571 |
| Fields | Biochemistry, Genetics and Molecular Biology,Neuroscience |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2762268528 |
| PMID | 28984810 |
| Type | article |
| Year | 2017 |

## Paper authors

- [Pavlína Plevová](https://scholariq.org/researchers/pavlina-plevova/)

## Paper primary topic

- [Hearing, Cochlea, Tinnitus, Genetics](https://scholariq.org/topics/hearing-cochlea-tinnitus-genetics/)

## Paper topics

- [Hearing, Cochlea, Tinnitus, Genetics](https://scholariq.org/topics/hearing-cochlea-tinnitus-genetics/)
- [Vestibular and auditory disorders](https://scholariq.org/topics/vestibular-and-auditory-disorders/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.