Absence of NFASC isoform NF186 causes an autosomal recessive ataxia syndromeM. Kvarnung, M. Shahsavani,F. Taylan, N. Breeuwsma,L. Laan,J. Schuster, Z. Jin,D. Nilsson,A. Lieden,B. Anderlid,M. Nordenskjold,E. Syk Lundberg,B. Birnir,N. Dahl,A. Nordgren,A. Lindstrand,A. FalkEUROPEAN JOURNAL OF HUMAN GENETICS(2019)引用 0|浏览52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