Clinical Manifestations Associated With the N-Terminal-Acetyltransferase NAA10 Gene Mutation in a Girl: Ogden Syndrome

Published 2017 View Full Article

Authors

Keywords

Ogden syndrome, genetic syndrome, X-linked condition, acetyltransferase, NAA10, gene, evolving neurological condition, movement disorder, hypersomnolence, levodopa

Journal

PEDIATRIC NEUROLOGY

Volume 76, Issue -, Pages 82-85

Publisher

Elsevier BV

Online

2017-07-20

DOI

10.1016/j.pediatrneurol.2017.07.010

Ask authors/readers for more resources

Protocol

Community support

Reagent

Community support

Reprint

Contact the author

Find the ideal target journal for your manuscript

Explore over 38,000 international journals covering a vast array of academic fields.

Ask a Question. Answer a Question.

Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.

Get Started