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About this Biochemistry, Genetics and Molecular Biology article
Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology by Lahbib, Saida; Leblond, Claire S.; Hamza, Mariem; Regnault, Béatrice; Lemée, Laure; Mathieu, Alexandre; Jaouadi, Hager; Mkaouar, Rahma; Youssef-Turki, Ilhem Ben; Belhadj, Ahlem; Kraoua, Ichraf; Bourgeron, Thomas; Abdelhak, Sonia is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Lahbib, Saida; Leblond, Claire S.; Hamza, Mariem; Regnault, Béatrice; Lemée, Laure; Mathieu, Alexandre; Jaouadi, Hager; Mkaouar, Rahma; Youssef-Turki, Ilhem Ben; Belhadj, Ahlem; Kraoua, Ichraf; Bourgeron, Thomas; Abdelhak, Sonia
- Publisher
- Springer-Verlag; Springer Verlag; Springer Science and Business Media LLC (ISSN 1234-1983)
- Published
- 2018
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)