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Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G &gt; T variant

Year of publication

2022

Authors

Bharadwaj, Thashi; Schrauwen, Isabelle; Acharya, Anushree; Nouel-Saied, Liz M.; Väisänen, Marja-Leena; Kraatari, Minna; Rahikkala, Elisa; Jarvela, Irma; Kotimäki, Jouko; Leal, Suzanne M.

Organizations and authors

University of Oulu

Rahikkala Elisa Orcid -palvelun logo

Kraatari-Tiri Minna

University of Helsinki

Jarvela Irma

Publication type

Publication format

Article

Parent publication type

Journal

Article type

Original article

Audience

Scientific

Peer-reviewed

Peer-Reviewed

MINEDU's publication type classification code

A1 Journal article (refereed), original research

Publication channel information

Journal

Molecular genetics & genomic medicine

Parent publication name

Molecular Genetics & Genomic Medicine

Volume

10

Issue

3

Article number

1866

ISSN

2324-9269

​Publication forum

82670

​Publication forum level

1

Open access

Open access in the publisher’s service

Yes

Open access of publication channel

Fully open publication channel

Self-archived

Yes

License of the self-archived publication

CC BY

Other information

Fields of science

Genetics, developmental biology, physiology; Biomedicine; Otorhinolaryngology, ophthalmology

Keywords

[object Object],[object Object],[object Object]

Publication country

United States

Internationality of the publisher

International

Language

English

International co-publication

Yes

Co-publication with a company

No

DOI

10.1002/mgg3.1866

The publication is included in the Ministry of Education and Culture’s Publication data collection

Yes