文献检索/Therapeutics and Clinical Risk ManagementEM-T3Therapeutics and Clinical Risk Management2015-04-01第 11 卷，635-635开放获取A novel missense KIT mutation causing piebaldism in one Chinese family associated with café-au-lait macules and intertriginous frecklingChengrang LiChinese Academy of Medical Sciences & Peking Union Medical CollegeWeixue JiaChinese Academy of Medical Sciences & Peking Union Medical CollegeXuemin XiaoChinese Academy of Medical Sciences & Peking Union Medical CollegeJianbing WuChinese Academy of Medical Sciences & Peking Union Medical CollegeYi-Ping MaChinese Academy of Medical Sciences & Peking Union Medical CollegeYiping GeChinese Academy of Medical Sciences & Peking Union Medical CollegeLi QiChinese Academy of Medical Sciences & Peking Union Medical CollegeQiuxia MaoChinese Academy of Medical Sciences & Peking Union Medical College开放获取全文去出版社页面 引用论文图谱收藏 被引提醒分享打印登录后看摘要和中文要点英文摘要、AI 生成的中文摘要和三条要点、参考文献和引证文献列表、论文图谱，注册免费。登录 / 注册关键词piebaldismKIT genemissense mutationscafé-au-lait spotsgenodermatosisneurofibromatosis type 1NF1 geneautosomal dominant inheritancewhite forelockdepigmentationChinese family参考文献13引证文献0相似文献引文网络关联作者相关机构登录后可以看完整列表。去登录论文图谱本篇和它的参考文献、引证文献、相似文献登录后可以看这篇的论文图谱：谁被它引用、谁引用了它、还有哪些相似的研究。登录 / 注册
