A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Barbara Vona, Neda Mazaheri, Sheng-Jia Lin, Lucy A. Dunbar, Reza Maroofian, Hela Azaiez, Kevin T. Booth, Sandrine Vitry, Aboulfazl Rad, Franz Rüschendorf, Pratishtha Varshney, Ben Fowler, Christian Beetz, Kumar N. Alagramam, David Murphy, Gholamreza Shariati, Alireza Sedaghat, Henry Houlden, Cassidy Petree, Shruthi VijayKumar, Richard J. H. Smith, Thomas Haaf, Aziz El-Amraoui, Michael R. Bowl, Gaurav K. Varshney, Hamid Galehdari

Open source

DOI: 10.1007/s00439-020-02254-z
Published: 2021-01-26
Container: Human Genetics
Publisher: Springer Science and Business Media LLC
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1007/s00439-020-02254-z,
  title = {A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans},
  author = {Barbara Vona and Neda Mazaheri and Sheng-Jia Lin and Lucy A. Dunbar and Reza Maroofian and Hela Azaiez and Kevin T. Booth and Sandrine Vitry and Aboulfazl Rad and Franz Rüschendorf and Pratishtha Varshney and Ben Fowler and Christian Beetz and Kumar N. Alagramam and David Murphy and Gholamreza Shariati and Alireza Sedaghat and Henry Houlden and Cassidy Petree and Shruthi VijayKumar and Richard J. H. Smith and Thomas Haaf and Aziz El-Amraoui and Michael R. Bowl and Gaurav K. Varshney and Hamid Galehdari},
  year = {2021},
  journal = {Human Genetics},
  doi = {10.1007/s00439-020-02254-z},
  url = {https://doi.org/10.1007/s00439-020-02254-z}
}

RIS

TY  - JOUR
TI  - A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
AU  - Barbara Vona
AU  - Neda Mazaheri
AU  - Sheng-Jia Lin
AU  - Lucy A. Dunbar
AU  - Reza Maroofian
AU  - Hela Azaiez
AU  - Kevin T. Booth
AU  - Sandrine Vitry
AU  - Aboulfazl Rad
AU  - Franz Rüschendorf
AU  - Pratishtha Varshney
AU  - Ben Fowler
AU  - Christian Beetz
AU  - Kumar N. Alagramam
AU  - David Murphy
AU  - Gholamreza Shariati
AU  - Alireza Sedaghat
AU  - Henry Houlden
AU  - Cassidy Petree
AU  - Shruthi VijayKumar
AU  - Richard J. H. Smith
AU  - Thomas Haaf
AU  - Aziz El-Amraoui
AU  - Michael R. Bowl
AU  - Gaurav K. Varshney
AU  - Hamid Galehdari
PY  - 2021
JO  - Human Genetics
DO  - 10.1007/s00439-020-02254-z
UR  - https://doi.org/10.1007/s00439-020-02254-z
ER  -

APA

Vona, B., Mazaheri, N., Lin, S., Dunbar, L. A., Maroofian, R., Azaiez, H., Booth, K. T., Vitry, S., Rad, A., Rüschendorf, F., Varshney, P., Fowler, B., Beetz, C., Alagramam, K. N., Murphy, D., Shariati, G., Sedaghat, A., Houlden, H., Petree, C., VijayKumar, S., Smith, R. J. H., Haaf, T., El-Amraoui, A., Bowl, M. R., Varshney, G. K., & Galehdari, H. (2021). A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans. Human Genetics. https://doi.org/10.1007/s00439-020-02254-z

Source records

crossref · retrieved 2026-09-26T15:45:19.668Z