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

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

37

Citations

6

References

2006

Year

William Wallefeld, Sabine Krause, Kristen L. Nowak, Danielle E. Dye, Rita Horváth, Zoltán Molnár, Miklós Szabó, Kazuhiro Hashimoto, Cristina Reina, Jose De Carlos,

Neuromuscular Disorders

Muscle FunctionMuscle InjurySkeletal MuscleMedicineGeneticsPathologyStop CodonCytoskeletonCommon DiseasesNeuromuscular PathologyNeuromusculoskeletal DisorderSevere Nemaline Myopathy

References

	Year	Citations

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