Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel

Author:

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

Funder

National Institute on Deafness and Other Communication Disorders

National Hospital Organization

Instituto de Salud Carlos III

Publisher

Elsevier BV

Subject

Genetics (clinical)

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