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Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant

Crossref DOI link: https://doi.org/10.1186/s13023-020-01508-3

Published Online: 2020-08-26

Published Print: 2020-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Safka Brozkova, Dana https://orcid.org/0000-0002-0572-7239
Varga, Lukas

Uhrova Meszarosova, Anna

Slobodova, Zuzana

Skopkova, Martina

Soltysova, Andrea

Ficek, Andrej

Jencik, Jan

Lastuvkova, Jana

Gasperikova, Daniela

Seeman, Pavel
Funding

Funding for this research was provided by:

Agentura Pro Zdravotnický Výzkum České Republiky (15-31899A)

Ministerstvo Zdravotnictví Ceské Republiky (00064203)

Agentúra na Podporu Výskumu a Vývoja (15–0067)

Agentúra na Podporu Výskumu a Vývoja (17-0296)

Grantová Agentura, Univerzita Karlova (1/0214/16)
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Text and Data Mining valid from 2020-08-26

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Article History

Received: 15 June 2020

Accepted: 13 August 2020

First Online: 26 August 2020

Ethics approval and consent to participate

: The ethics committee of University Hospital Motol approved the examination (ID 15-31899A).

: The authors affirm that human research participants provided informed consent for publication of the images in Fig.a.

: The authors declare that they have no conflict of interests.

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