PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive CharcotMarieTooth disease

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PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive CharcotMarieTooth disease

Author: Azzedine, Hamid; Zavadakova, Petra; Plante-Bordeneuve, Violaine; Pato, Maria Vaz; Pinto, Nuno; Bartesaghi, Luca; Zenker, Jennifer; Poirot, Olivier; Bernard-Marissal, Nathalie; Gouttenoire, Estelle Arnaud; Cartoni, Romain; Title, Alexandra; Venturini, Giulia; Medard, Jean-Jacques; Makowski, Edward; Schoels, Ludger; Claeys, Kristl G.; Stendel, Claudia; Roos, Andreas; Weis, Joachim; Dubourg, Odile; Loureiro, Jose Leal; Stevanin, Giovanni; Said, Gerard; Amato, Anthony; Baraban, Jay; LeGuern, Eric; Senderek, Jan; Rivolta, Carlo; Chrast, Roman
Tübinger Autor(en):
Schöls, Ludger
Published in: Human Molecular Genetics (2013), Bd. 22, H. 20, S. 4224-4232
Verlagsangabe: Oxford Univ Press
Language: English
Full text: http://dx.doi.org/10.1093/hmg/ddt274
ISSN: 0964-6906
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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