Hypocitrullinemia on Newborn Screening as an early indicator of Leigh Syndrome due to homoplasmic m.8993T > G variant R. Treitel,E. Moore, J. McLaughlin,M. FrigeniANNALS OF NEUROLOGY(2022)引用 0|浏览0暂无评分关键词Genetics, Rare DiseasesAI 理解论文溯源树样例生成溯源树,研究论文发展脉络Chat Paper正在生成论文摘要