The noncoding genome and hearing loss.

Avraham, Karen B; Khalaily, Lama; Noy, Yael; Kamal, Lara; Koffler-Brill, Tal; Taiber, Shahar

Avraham, Karen B; Khalaily, Lama; Noy, Yael; Kamal, Lara; Koffler-Brill, Tal; Taiber, Shahar.

Afiliação

Avraham KB; Department of Human Molecular Genetics and Biochemistry, Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, 6997801, Tel Aviv, Israel. karena@tauex.tau.ac.il.
Khalaily L; Department of Human Molecular Genetics and Biochemistry, Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, 6997801, Tel Aviv, Israel.
Noy Y; Department of Human Molecular Genetics and Biochemistry, Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, 6997801, Tel Aviv, Israel.
Kamal L; Department of Human Molecular Genetics and Biochemistry, Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, 6997801, Tel Aviv, Israel.
Koffler-Brill T; Department of Human Molecular Genetics and Biochemistry, Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, 6997801, Tel Aviv, Israel.
Taiber S; Department of Human Molecular Genetics and Biochemistry, Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, 6997801, Tel Aviv, Israel.

Hum Genet ; 141(3-4): 323-333, 2022 Apr.

Article em En | MEDLINE | ID: mdl-34491412

Assuntos

Surdez; Perda Auditiva; MicroRNAs; RNA Longo não Codificante; Surdez/genética; Genoma Humano; Perda Auditiva/genética; Humanos; MicroRNAs/genética; RNA Longo não Codificante/genética

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Surdez / MicroRNAs / RNA Longo não Codificante / Perda Auditiva Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Israel

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