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About this Biochemistry, Genetics and Molecular Biology article
A novel biallelic loss‐of‐function mutation in TMCO1 gene confirming and expanding the phenotype spectrum of cerebro‐facio‐thoracic dysplasia by Sharkia, Rajech; Zalan, Abdelnaser; Jabareen‐Masri, Azhar; Hengel, Holger; Schöls, Ludger; Kessel, Amit; Azem, Abdussalam; Mahajnah, Muhammad 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
- Sharkia, Rajech; Zalan, Abdelnaser; Jabareen‐Masri, Azhar; Hengel, Holger; Schöls, Ludger; Kessel, Amit; Azem, Abdussalam; Mahajnah, Muhammad
- Publisher
- John Wiley and Sons; Wiley (John Wiley & Sons); Wiley-Liss Inc; Wiley (ISSN 1552-4825)
- Published
- 2019
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)