A Novel Heterozygous Missense Variant (c.667G>T;p.Gly223Cys) in <i>USH1C</i> That Interferes With Cadherin-Related 23 and Harmonin Interaction Causes Autosomal Dominant Nonsyndromic Hearing Loss.
- DOI
- 10.3343/alm.2020.40.3.224
- Published
- 2020-05-01
- Container
- Ann Lab Med
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3343/alm.2020.40.3.224,
title = {A Novel Heterozygous Missense Variant (c.667G>T;p.Gly223Cys) in <i>USH1C</i> That Interferes With Cadherin-Related 23 and Harmonin Interaction Causes Autosomal Dominant Nonsyndromic Hearing Loss.},
author = {Song JS and Bahloul A and Petit C and Kim SJ and Moon IJ and Lee J and Ki CS.},
year = {2020},
journal = {Ann Lab Med},
doi = {10.3343/alm.2020.40.3.224},
url = {https://doi.org/10.3343/alm.2020.40.3.224}
}RIS
TY - JOUR TI - A Novel Heterozygous Missense Variant (c.667G>T;p.Gly223Cys) in <i>USH1C</i> That Interferes With Cadherin-Related 23 and Harmonin Interaction Causes Autosomal Dominant Nonsyndromic Hearing Loss. AU - Song JS AU - Bahloul A AU - Petit C AU - Kim SJ AU - Moon IJ AU - Lee J AU - Ki CS. PY - 2020 JO - Ann Lab Med DO - 10.3343/alm.2020.40.3.224 UR - https://doi.org/10.3343/alm.2020.40.3.224 ER -
APA
JS, S., A, B., C, P., SJ, K., IJ, M., J, L., & CS., K. (2020). A Novel Heterozygous Missense Variant (c.667G>T;p.Gly223Cys) in <i>USH1C</i> That Interferes With Cadherin-Related 23 and Harmonin Interaction Causes Autosomal Dominant Nonsyndromic Hearing Loss.. Ann Lab Med. https://doi.org/10.3343/alm.2020.40.3.224
Source records
- europe-pmc · retrieved 2026-09-25T06:50:37.707Z