Titel

Merkliste
1 Ergebnisse

De novo variants of CSNK2B cause a new intellectual disabil..:

Maria Asif ; Emrah Kaygusuz ; Marwan Shinawi...
http://www.sciencedirect.com/science/article/pii/S2666247722000276. , 2022

Link: https://doi.org/10.1016/j.xhgg.2022.100111

RT Journal
T1 <Title>De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:9ab8572fe2874d66a9f70e678cec119a&Exemplar=1&LAN=DE
				
A1 Maria Asif
A1 Emrah Kaygusuz
A1 Marwan Shinawi
A1 Anna Nickelsen
A1 Tzung-Chien Hsieh
A1 Prerana Wagle
A1 Birgit S. Budde
A1 Jennifer Hochscherf
A1 Uzma Abdullah
A1 Stefan Höning
A1 Christian Nienberg
A1 Dirk Lindenblatt
A1 Angelika A. Noegel
A1 Janine Altmüller
A1 Holger Thiele
A1 Susanne Motameny
A1 Nicole Fleischer
A1 Idan Segal
A1 Lynn Pais
A1 Sigrid Tinschert
A1 Nadra Nasser Samra
A1 Juliann M. Savatt
A1 Natasha L. Rudy
A1 Chiara De Luca
A1 Paola Fortugno
A1 Susan M. White
A1 Peter Krawitz
A1 Anna C.E. Hurst
A1 Karsten Niefind
A1 Joachim Jose
A1 Francesco Brancati
A1 Peter Nürnberg
A1 Muhammad Sajid Hussain
PB Elsevier
YR 2022
K1 intellectual disability-craniodigital syndrome
K1 CSNK2B
K1 CK2β
K1 CK2
K1 Wnt signaling
K1 β-catenin
K1 Genetics
K1 QH426-470
JF http://www.sciencedirect.com/science/article/pii/S2666247722000276
LK http://dx.doi.org/https://doi.org/10.1016/j.xhgg.2022.100111
DO https://doi.org/10.1016/j.xhgg.2022.100111
SF ELIB - SuUB Bremen

Export

RefWorks (nur Desktop-Version!)
Flow (Zuerst in Flow einloggen, dann importieren)