Gene expression profiling identifies molecular pathways associated with collagen VI deficiency and provides novel therapeutic targets.

Ullrich congenital muscular dystrophy (UCMD), caused by collagen VI deficiency, is a common congenital muscular dystrophy. At present, the role of collagen VI in muscle and the mechanism of disease are not fully understood. To address this we have applied microarrays to analyse the transcriptome of...

Fuld beskrivelse

Bibliografiske detaljer

Principais autores:	Sonia Paco, Susana G Kalko, Cristina Jou, María A Rodríguez, Joan Corbera, Francesco Muntoni, Lucy Feng, Eloy Rivas, Ferran Torner, Francesca Gualandi, Anna M Gomez-Foix, Anna Ferrer, Carlos Ortez, Andrés Nascimento, Jaume Colomer, Cecilia Jimenez-Mallebrera
Format:	Artigo
Sprog:	Inglês
Udgivet:	Public Library of Science (PLoS) 2013-01-01
Serier:	PLoS ONE
Online adgang:	https://doi.org/10.1371/journal.pone.0077430
Tags:	Tilføj Tag Ingen Tags, Vær først til at tagge denne postø!