Further evidence that biallelic nonsense variants in ATL1 cause complicated hereditary spastic paraplegia

Kraft, Florian; Begemann, Matthias; Lischka, Annette; Häusler, Martin Georg; Holschbach, Petra Beatrix; Elbracht, Miriam; Franken, Lena; Kurth, Ingo; Lausberg, Eva; Eggermann, Katja; Knopp, Cordula; Pappa, Angeliki

doi:1018-4813

Further evidence that biallelic nonsense variants in ATL1 cause complicated hereditary spastic paraplegia

Kraft, Florian^RWTH* ; Begemann, Matthias^RWTH* ; Lausberg, Eva^RWTH* ; Lischka, Annette^RWTH* ; Holschbach, Petra Beatrix^RWTH* ; Pappa, Angeliki^RWTH* ; Franken, Lena^RWTH* ; Elbracht, Miriam^RWTH* ; Eggermann, Katja^RWTH* ; Häusler, Martin Georg^RWTH* ; Kurth, Ingo^RWTH* ; Knopp, Cordula^RWTH*

In
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference

In
European journal of human genetics 32(Supplement 1), Seiten/Artikel-Nr.:EP10.049

2024

Konferenz/Event:56. European Society of Human Genetics (ESHG) Conference , Glasgow , UK , 2023-06-10 - 2023-06-13

ImpressumBasingstoke : Stockton Press

Umfang209-209

ISSN1476-5438

Poster abstract

Online
URL: https://doi.org/10.1038/s41431-023-01481-y

Einrichtungen

External link:

Homepage of journal

Dokumenttyp
Abstract/Journal Article/Contribution to a conference proceedings

Format
online, print

Sprache
English

Externe Identnummern
WOS Core Collection: WOS:001147414900569

Interne Identnummern
RWTH-CONV-253765
Datensatz-ID: 1007390

Beteiligte Länder
Germany

Lizenzstatus der Zeitschrift

; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DEAL Springer ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 5 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection