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A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58. [electronic resource] by
- Lezirovitz, Karina
- Vieira-Silva, Gleiciele A
- Batissoco, Ana C
- Levy, Débora
- Kitajima, Joao P
- Trouillet, Alix
- Ouyang, Ellen
- Zebarjadi, Navid
- Sampaio-Silva, Juliana
- Pedroso-Campos, Vinicius
- Nascimento, Larissa R
- Sonoda, Cindy Y
- Borges, Vinícius M
- Vasconcelos, Laura G
- Beck, Roberto M O
- Grasel, Signe S
- Jagger, Daniel J
- Grillet, Nicolas
- Bento, Ricardo F
- Mingroni-Netto, Regina C
- Oiticica, Jeanne
Producer: 20210812
In:
Human molecular genetics vol. 29
Availability: No items available.
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