First reported CABP2-related non-syndromic hearing loss in Northern Europe

Inger Norlyk Sheyanth; Allan Thomas Højland; Henrik Okkels; Ihab Lolas; Christian Thorup; Michael Bjørn Petersen

doi:10.1002/mgg3.1639

First reported CABP2-related non-syndromic hearing loss in Northern Europe

Inger Norlyk Sheyanth^*, Allan Thomas Højland, Henrik Okkels, Ihab Lolas, Christian Thorup, Michael Bjørn Petersen

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Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

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Originalsprog	Engelsk
Artikelnummer	e1639
Tidsskrift	Molecular Genetics and Genomic Medicine
Vol/bind	9
Udgave nummer	4
Antal sider	5
ISSN	2324-9269
DOI	https://doi.org/10.1002/mgg3.1639
Status	Udgivet - apr. 2021

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10.1002/mgg3.1639Licens: CC BY-NC-ND 4.0

Sheyanth et al. (2021) First reported CABP2-related non-syndromic hearing loss in Northern EuropeForlagets udgivne version, 515 KBLicens: CC BY-NC-ND 4.0

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@article{6f5a515593af485d8570965909356c05,

title = "First reported CABP2-related non-syndromic hearing loss in Northern Europe",

keywords = "autosomal recessive, CABP2, hearing loss",

author = "Sheyanth, {Inger Norlyk} and H{\o}jland, {Allan Thomas} and Henrik Okkels and Ihab Lolas and Christian Thorup and Petersen, {Michael Bj{\o}rn}",

note = "{\textcopyright} 2021 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC.",

year = "2021",

month = apr,

doi = "10.1002/mgg3.1639",

language = "English",

volume = "9",

journal = "Molecular Genetics & Genomic Medicine",

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TY - JOUR

T1 - First reported CABP2-related non-syndromic hearing loss in Northern Europe

AU - Sheyanth, Inger Norlyk

AU - Højland, Allan Thomas

AU - Okkels, Henrik

AU - Lolas, Ihab

AU - Thorup, Christian

AU - Petersen, Michael Bjørn

PY - 2021/4

Y1 - 2021/4

KW - autosomal recessive

KW - CABP2

KW - hearing loss

UR - http://www.scopus.com/inward/record.url?scp=85101989140&partnerID=8YFLogxK

U2 - 10.1002/mgg3.1639

DO - 10.1002/mgg3.1639

M3 - Journal article

C2 - 33666369

AN - SCOPUS:85101989140

VL - 9

JO - Molecular Genetics & Genomic Medicine

JF - Molecular Genetics & Genomic Medicine

SN - 2324-9269

IS - 4

M1 - e1639

ER -

First reported CABP2-related non-syndromic hearing loss in Northern Europe

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