Mitochondrial DNA depletion syndrome in a newborn with Jaundice Caused by DGUOK mutation and complete uniparental disomy of chromosome 2

• Principais autores: Jun-ke Xia (Autor), Zhou-xian Bai (Autor), Xue-chao Zhao (Autor), Jing-jing Meng (Autor), Chen Chen (Autor), Xiang-dong Kong (Autor)
• Formato: Livro
• Publicado em: Elsevier, 2020-10-01T00:00:00Z.
• Assuntos: article
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