Development of autoantibodies against muscle-specific FHL1 in severe inflammatory myopathies

Mutations of the gene encoding four-and-a-half LIM domain 1 (FHL1) are the causative factor of several X-linked hereditary myopathies that are collectively termed FHL1-related myopathies. These disorders are characterized by severe muscle dysfunction and damage. Here, we have shown that patients wit...

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Détails bibliographiques
Publié dans:J Clin Invest
Auteurs principaux: Albrecht, Inka, Wick, Cecilia, Hallgren, Åsa, Tjärnlund, Anna, Nagaraju, Kanneboyina, Andrade, Felipe, Thompson, Kathryn, Coley, William, Phadke, Aditi, Diaz-Gallo, Lina-Marcela, Bottai, Matteo, Nennesmo, Inger, Chemin, Karine, Herrath, Jessica, Johansson, Karin, Wikberg, Anders, Ytterberg, A. Jimmy, Zubarev, Roman A., Danielsson, Olof, Krystufkova, Olga, Vencovsky, Jiri, Landegren, Nils, Wahren-Herlenius, Marie, Padyukov, Leonid, Kämpe, Olle, Lundberg, Ingrid E.
Format: Artigo
Langue:Inglês
Publié: American Society for Clinical Investigation 2015
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4665781/
https://ncbi.nlm.nih.gov/pubmed/26551678
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI81031
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