Fetal akinesia caused by a novel actin filament aggregate myopathy skeletal muscle actin gene (ACTA1) mutation

W. Stenzel, S. Prokop, W. Kress, S. Huppmann, A. Loui, N.M.E. Sarioglu, Nigel Laing, J.C. Sparrow, F.L. Heppner, H.H. Goebel

Research output: Contribution to journalArticle

9 Citations (Scopus)
Original languageEnglish
Pages (from-to)531-533
JournalNeuromuscular Disorders
Volume20
DOIs
Publication statusPublished - 2010

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