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Elsevier, Neuromuscular Disorders, 9-10(16), p. 541-547, 2006

DOI: 10.1016/j.nmd.2006.07.018

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Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1)

Journal article published in 2006 by William Wallefeld, Sabine Krause, Kristen J. Nowak, Danielle Dye, Rita Horváth, Zoltán Molnár, Miklós Szabó, Kazuhiro Hashimoto, Cristina Reina, Jose De Carlos, Jordi Rosell, Ana Cabello, Carmen Navarro, Ichizo Nishino ORCID, Hanns Lochmüller and other authors.
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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