Author: "Prehl I" / Topic: channelopathy - Searchworks@Jio Institute Digital Library Search Results

Searchworks

Select search scope, currently: Articles

Catalog

books, media & more in Jio Institute collections

Articles

journal articles & other e-resources

Your search keyword '"Prehl I"' showing total 1 results

Start Over Author "Prehl I" Topic channelopathy

1 results on '"Prehl I"'

1. Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia

Author: Schwarz, N., Hahn, A., Bast, T., Müller, S., Löffler, H., Maljevic, S., Gaily, E., Prehl, I., Biskup, S., Joensuu, T., Lehesjoki, A.-E., Neubauer, B. A., Lerche, H., and Hedrich, U. B. S.
Published: 2016
Full Text: View/download PDF

Catalog

Books, media, physical & digital resources

See catalog results