Novel VPS33B mutation in a patient with autosomal recessive keratoderma-ichthyosis-deafness (ARKID) syndromeS. Alter,A. Hotz,A. Jahn,N. Di Donato,E. Schroeck,M. Smitka,M. von der Hagen,J. Schallner,M. Menschikowski, C. Gillitzer,M. W. Laass,J. Fischer,A. TzschachEUROPEAN JOURNAL OF HUMAN GENETICS(2019)引用 6|浏览23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