EGR2 mutation enhances phenotype spectrum of Dejerine–Sottas syndromeElena Gargaun,Andreea Mihaela Seferian, Ruxandra Cardas,Anne-Gaelle Le Moing,Catherine Delanoe,Juliette Nectoux,Isabelle Nelson,Gisèle Bonne,Marie-Thérèse Bihoreau,Jean-François Deleuze,Anne Boland,Cécile Masson,Laurent Servais,Teresa GidaroJournal of neurology（2016）引用 5|浏览25暂无评分关键词Riboflavin, Compound Muscle Action Potential, Facial Weakness, Musculocutaneous Nerve, SMN1 GeneAI 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
