Adaptive protein synthesis in genetic models of copper deficiency and childhood neurodegeneration.

• Tác giả: Alina Baiju, Shatabdi Bhattacharjee, Lauren B Clayton, Daniel N Cox, Duc M Duong, Victor Faundez, Avanti Gokhale, Alicia R Lane, William L Liu, Mike McKenna, Felix G Rivera Moctezuma, Atit A Patel, Anupam Patgiri, Michael J Petris, Anne M Roberts, Blaine R Roberts, Noah E Scher, Kaela S Singleton, Tommy Tran, Alysia D Vrailas-Mortimer, Erica Werner, Levi B Wood, Stephanie A Zlatic
• Ngôn ngữ: eng
• Ký hiệu phân loại: 996.4 +Line Islands (Equatorial Islands)
• Thông tin xuất bản: United States : Molecular biology of the cell , 2025
• Bộ sưu tập: NCBI
• ID: 62091

Tóm tắt

Rare inherited diseases caused by mutations in the copper transporters