当前位置:
X-MOL 学术
›
J. Hum. Genet.
›
论文详情
Our official English website, www.x-mol.net, welcomes your
feedback! (Note: you will need to create a separate account there.)
Corrigendum: Novel KCNB1 mutation associated with non-syndromic intellectual disability.
Journal of Human Genetics ( IF 2.6 ) Pub Date : 2017-04-26 , DOI: 10.1038/jhg.2017.17 Xénia Latypova , Naomichi Matsumoto , Cécile Vinceslas-Muller , Stéphane Bézieau , Bertrand Isidor , Noriko Miyake
中文翻译:
更正:与非综合征性智力障碍相关的新型KCNB1突变。
更新日期:2019-11-01
Journal of Human Genetics ( IF 2.6 ) Pub Date : 2017-04-26 , DOI: 10.1038/jhg.2017.17 Xénia Latypova , Naomichi Matsumoto , Cécile Vinceslas-Muller , Stéphane Bézieau , Bertrand Isidor , Noriko Miyake
中文翻译:
更正:与非综合征性智力障碍相关的新型KCNB1突变。