Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

A Novel Exon 1 Mutation in a Patient with Atypical Lafora Progressive Myoclonus Epilepsy Seen as Childhood‐onset Cognitive Deficit

Title: A Novel Exon 1 Mutation in a Patient with Atypical Lafora Progressive Myoclonus Epilepsy Seen as Childhood‐onset Cognitive Deficit
Authors: Annesi, Grazia; Sofia, Vito; Gambardella, Antonio; Candiano, Innocenza C. Cirò; Spadafora, Patrizia; Annesi, Ferdinanda; Cutuli, Nunzio; De Marco, Elvira V.; Civitelli, Donatella; Carrideo, Sara; Tarantino, Patrizia; Barone, Rita; Zappia, Mario; Quattrone, Aldo
Source: Epilepsia ; volume 45, issue 3, page 294-295 ; ISSN 0013-9580 1528-1167
Publisher Information: Wiley
Publication Year: 2004
Collection: Wiley Online Library (Open Access Articles via Crossref)
Document Type: article in journal/newspaper
Language: English
DOI: 10.1111/j.0013-9580.2004.33203.x
Availability: http://dx.doi.org/10.1111/j.0013-9580.2004.33203.x; https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.0013-9580.2004.33203.x; https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.0013-9580.2004.33203.x; https://onlinelibrary.wiley.com/doi/full-xml/10.1111/j.0013-9580.2004.33203.x
Rights: http://onlinelibrary.wiley.com/termsAndConditions#vor
Accession Number: edsbas.6138F97C
Database: BASE