دورية أكاديمية

Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

التفاصيل البيبلوغرافية
العنوان: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
المؤلفون: Jin, Sheng ChihAff1, Aff2, Aff3, Lewis, Sara A.Aff4, Aff5, Bakhtiari, SomayehAff4, Aff5, Zeng, XueAff1, Aff2, Sierant, Michael C.Aff1, Aff2, Shetty, SheetalAff4, Aff5, Nordlie, Sandra M.Aff4, Aff5, Elie, AurelianeAff4, Aff5, Corbett, Mark A., Norton, Bethany Y.Aff4, Aff5, van Eyk, Clare L., Haider, Shozeb, Guida, Brandon S.Aff4, Aff5, Magee, HelenAff4, Aff5, Liu, JamesAff4, Aff5, Pastore, Stephen, Vincent, John B., Brunstrom-Hernandez, Janice, Papavasileiou, Antigone, Fahey, Michael C., Berry, Jesia G., Harper, Kelly, Zhou, Chongchen, Zhang, Junhui, Li, Boyang, Zhao, Hongyu, Heim, Jennifer, Webber, Dani L., Frank, Mahalia S. B., Xia, Lei, Xu, Yiran, Zhu, Dengna, Zhang, Bohao, Sheth, Amar H., Knight, James R., Castaldi, Christopher, Tikhonova, Irina R., López-Giráldez, Francesc, Keren, Boris, Whalen, Sandra, Buratti, Julien, Doummar, Diane, Cho, Megan, Retterer, Kyle, Millan, Francisca, Wang, Yangong, Waugh, Jeff L., Rodan, Lance, Cohen, Julie S., Fatemi, Ali, Lin, Angela E., Phillips, John P., Feyma, Timothy, MacLennan, Suzanna C., Vaughan, Spencer, Crompton, Kylie E., Reid, Susan M., Reddihough, Dinah S., Shang, Qing, Gao, Chao, Novak, Iona, Badawi, Nadia, Wilson, Yana A., McIntyre, Sarah J., Mane, Shrikant M., Wang, XiaoyangAff14, Aff32, Amor, David J., Zarnescu, Daniela C., Lu, Qiongshi, Xing, Qinghe, Zhu, ChanglianAff14, Aff32, Bilguvar, KayaAff1, Aff15, Padilla-Lopez, SergioAff4, Aff5, Lifton, Richard P.Aff1, Aff2, Gecz, Jozef, MacLennan, Alastair H., Kruer, Michael C.Aff4, Aff5, IDs4158802006951_cor77
المصدر: Nature Genetics. 52(10):1046-1056
قاعدة البيانات: Springer Nature Journals
الوصف
تدمد:10614036
15461718
DOI:10.1038/s41588-020-0695-1