Publication not explained
This publication has not yet been explained in plain language by the author(s). However, you can still read the publication.
If you are one of the authors, claim this publication so you can create a plain language summary to help more people find, understand and use it.
Featured Image
Read the Original
This page is a summary of: Early-onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1
and MAGEL2
, Epilepsia Open, November 2017, Wiley,
DOI: 10.1002/epi4.12085.
You can read the full text:
Contributors
The following have contributed to this page
