Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features-Reference-Cited by-同舟云学术

Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features

Published:2014-03-10 Issue:4 Volume:124 Page:1468-1482
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Tucci Valter,Kleefstra Tjitske,Hardy Andrea,Heise Ines,Maggi Silvia,Willemsen Marjolein H.,Hilton Helen,Esapa Chris,Simon Michelle,Buenavista Maria-Teresa,McGuffin Liam J.,Vizor Lucie,Dodero Luca,Tsaftaris Sotirios,Romero Rosario,Nillesen Willy N.,Vissers Lisenka E.L.M.,Kempers Marlies J.,Vulto-van Silfhout Anneke T.,Iqbal Zafar,Orlando Marta,Maccione Alessandro,Lassi Glenda,Farisello Pasqualina,Contestabile Andrea,Tinarelli Federico,Nieus Thierry,Raimondi Andrea,Greco Barbara,Cantatore Daniela,Gasparini Laura,Berdondini Luca,Bifone Angelo,Gozzi Alessandro,Wells Sara,Nolan Patrick M.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

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4. Cadherins and catenins in synapse development

5. The Structure of the β-Catenin/E-Cadherin Complex and the Molecular Basis of Diverse Ligand Recognition by β-Catenin

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