Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mechthild Stötter"'
Autor:
Sabine Rudnik-Schöneborn, Marc Gleichmann, Manfred Wehnert, Gisèle Bonne, Michel Mittelbronn, Rudolf Korinthenberg, Antje Bornemann, Frank Hanisch, Mechthild Stötter
Publikováno v:
Brain Pathol
UNLABELLED Autosomal dominant Emery-Dreifuss muscular dystrophy is caused by mutations in the LMNA gene that code for the nuclear membrane protein lamin A/C. We investigated skeletal muscle fibers from several muscles for cytoplasmic degenerative cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bc7b81e5a9457aa6931785d4192d8b0
https://doi.org/10.1111/j.1750-3639.2006.00028.x
https://doi.org/10.1111/j.1750-3639.2006.00028.x
Autor:
U.-P. Ketelsen, Mechthild Stötter, Antje Bornemann, Sven Laule, Richard Meyermann, Lars Wöckel
Publikováno v:
Acta Neuropathologica. 95:547-551
Centronuclear myopathy (CNM) is a congenital myopathy which manifests itself as a severe neonatal (also termed myotubular myopathy), early-onset, or adult form. The histological pattern of each is marked by a considerable number of nuclei of muscle f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c95b165a207c597e93e412efbaf31c8
https://doi.org/10.1007/s004010050836
https://doi.org/10.1007/s004010050836