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Autor:
Kathryn Thompson, Nils Landegren, A. Jimmy Ytterberg, Matteo Bottai, Jessica Herrath, Ingrid E. Lundberg, Cecilia Wick, Kanneboyina Nagaraju, Åsa Hallgren, Felipe Andrade, Jiri Vencovsky, Aditi Phadke, Roman A. Zubarev, Leonid Padyukov, Olof Danielsson, Lina-Marcela Diaz-Gallo, Inka Albrecht, Inger Nennesmo, Olga Krystufkova, Anna Tjärnlund, Marie Wahren-Herlenius, Olle Kämpe, Karine Chemin, Karin Johansson, William Coley, Anders Wikberg
Publikováno v:
The Journal of clinical investigation. 125(12)
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