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About this book
A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism by Shridhar Parthasarathy & Sarah McKeown Ruggiero & Antoinette Gelot & Fernanda C Soardi & Bethânia F R Ribeiro & Douglas E V Pires & David B Ascher & Alain Schmitt & Caroline Rambaud & Alfonso Represa & Hongbo M Xie & Laina Lusk & Olivia Wilmarth &... is a book available to read on EtoBox.
- Author
- Shridhar Parthasarathy & Sarah McKeown Ruggiero & Antoinette Gelot & Fernanda C Soardi & Bethânia F R Ribeiro & Douglas E V Pires & David B Ascher & Alain Schmitt & Caroline Rambaud & Alfonso Represa & Hongbo M Xie & Laina Lusk & Olivia Wilmarth &...
- Publisher
- American Society of Human Genetics
- Language
- EN
More by Shridhar Parthasarathy & Sarah McKeown Ruggiero & Antoinette Gelot & Fernanda C Soardi & Bethânia F R Ribeiro & Douglas E V Pires & David B Ascher & Alain Schmitt & Caroline Rambaud & Alfonso Represa & Hongbo M Xie & Laina Lusk & Olivia Wilmarth &...
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