A new inherited syndrome with severe neutropenia and neurological involvement due to autosomal recessive COPZ1 mutation N. Borbaran-Bravo, E. Deordieva, S. Braeuning, B. Dannenmann, L. Doll,M. ElGamacy,C. Zeidler, B. Bajoghly, A. Maschan,A. Shcherbina,K. Welte,J. Skokowa,M. KlimiankouKLINISCHE PADIATRIE（2022）引用 0|浏览6暂无评分AI 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
