Document is current
Any future updates will be listed below
-
Authors
Shen, Jun
Oza, Andrea M.
del Castillo, Ignacio
Duzkale, Hatice
Matsunaga, Tatsuo
Pandya, Arti
Kang, Hyunseok P.
Mar-Heyming, Rebecca
Guha, Saurav
Moyer, Krista
Lo, Christine
Kenna, Margaret
Alexander, John J.
Zhang, Yan
Hirsch, Yoel
Luo, Minjie
Cao, Ye
Wai Choy, Kwong
Cheng, Yen-Fu
Avraham, Karen B.
Hu, Xinhua
Garrido, Gema
Moreno-Pelayo, Miguel A.
Greinwald, John
Zhang, Kejian
Zeng, Yukun
Brownstein, Zippora
Basel-Salmon, Lina
Davidov, Bella
Frydman, Moshe
Weiden, Tzvi
Nagan, Narasimhan
Willis, Alecia
Hemphill, Sarah E.
Grant, Andrew R.
Siegert, Rebecca K.
DiStefano, Marina T.
Amr, Sami S.
Rehm, Heidi L.
Abou Tayoun, Ahmad N.
Azaiez, Hela
Booth, Kevin T.
Smith, Richard J.
Giersch, Anne B.
Morton, Cynthia C.
Liu, Xue Z.
Tekin, Mustafa
Lu, Yu
Yuan, Huijun
Mutai, Hideki
Schimmenti, Lisa
-
Funding
Funding for this research was provided by:
National Institute on Deafness and Other Communication Disorders (R03DC013866)
National Institute on Deafness and Other Communication Disorders (R01DC015052)
National Institute on Deafness and Other Communication Disorders (R01DC011835)
National Hospital Organization (H27-NHOkankaku-02)
Instituto de Salud Carlos III (PI14/01162)
Instituto de Salud Carlos III (PI14/0948)
- License Information
-
More Information
This article is maintained by: Elsevier
Article Title: Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0535-9
Content Type: article
Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics
