ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs

Author:

DiStefano Marina T.,Hemphill Sarah E.,Oza Andrea M.,Siegert Rebecca K.,Grant Andrew R.,Hughes Madeline Y.,Cushman Brandon J.,Azaiez Hela,Booth Kevin T.,Chapin Alex,Duzkale Hatice,Matsunaga Tatsuo,Shen Jun,Zhang Wenying,Kenna Margaret,Schimmenti Lisa A.,Tekin Mustafa,Rehm Heidi L.,Tayoun Ahmad N. Abou,Amr Sami S.,Abdelhak Sonia,Alexander John,Avraham Karen,Bhatia Neha,Bai Donglin,Boczek Nicole,Brownstein Zippora,Burt Rachel,Bylstra Yasmin,del Castillo Ignacio,Choi Byung Yoon,Downie Lilian,Friedman Thomas,Giersch Anne,Goh Jasmine,Greinwald John,Griffith Andrew J.,Hernandez Amy,Holt Jeffrey,Hosoya Makoto,Ying Lim Jiin,Jain Kanika,Kim Un-Kyung,Kremer Hannie,Krantz Ian,Leal Suzanne,Lewis Morag,Liu Xue Zhong,Low Wendy,Lu Yu,Luo Minjie,Masmoudi Saber,Ming Tan Yuen,Moreno-Pelayo Miguel Angel,Morín Matías,Morton Cynthia,Murray Jaclyn,Mutai Hideki,Nara Kiyomitsu,Pandya Arti,Pei-Rong Sylvia Kam,Smith Richard J.H.,Jamuar Saumya Shekhar,Suer Funda Elif,Usami Shin-Ichi,Van Camp Guy,Yamazawa Kazuki,Yuan Hui-Jun,Black-Zeigelbein Elizabeth,Zhang Keijan

Funder

National Human Genome Research Institute

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference28 articles.

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