Mip (Aqp0) Mutations In Humans: Associated With A Novel Locus For Autosomal Dominant Congenital Cataract.

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE(2000)

引用 0|浏览2
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