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Whole-exome sequencing suggests multiallelic inheritance for childhood-onset Ménière's disease

Year of publication

2019

Authors

Skarp, S.; Kanervo, L.; Kotimäki, J.; Sorri, M.; Männikkö, M.; Hietikko, E.

Organizations and authors

University of Oulu

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Sorri Martti

Oulu University Hospital Catchment Area

Sorri Martti

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

Annals of human genetics

Issue

6

Pages

389-396

ISSN

0003-4800

​Publication forum

51229

​Publication forum level

1

Open access

Open access in the publisher’s service

No

Self-archived

No

Other information

Fields of science

Biochemistry, cell and molecular biology; Otorhinolaryngology, ophthalmology

Keywords

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

Publication country

United Kingdom

Internationality of the publisher

International

Language

English

International co-publication

No

Co-publication with a company

No

DOI

10.1111/ahg.12327

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

Yes