论文信息 - A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism - 字舞流文

A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism

I. Helbig | B. Kennedy | A. Gelot | D. Ascher | A. Schmitt | S. Pena | F. C. Soardi | C. Rambaud | D. Pires | C. Mignot | B. Keren | C. Nava | B. Ribeiro | J. Buratti | V. Cuddapah | Benjamin C. Kennedy | Laina Lusk | D. Gras | Shridhar Parthasarathy | Sarah M Ruggiero | H. Xie | Olivia Wilmarth | Pamela Pojomovsky McDonnell | Olivia A Juarez | Alexandra N Grace | Samuel R Pierce | S. M. Ruggiero | S. Parthasarathy | O. Wilmarth | P. P. McDonnell