Author response for "A novel bi‐allelic loss‐of‐function mutation in STIM1 expands the phenotype of STIM1 ‐related diseases" Alexandra Salvi, Cristina Skrypnyk, Nathalie Da Silva, J. Andoni Urtizberea, Moiz Bakhiet, Catherine Robert, Nicolas Lévy, Andre Megarbané, Valerie Delague, Marc Bartolicrossref(2021)引用 0|浏览1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