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A TPM2 mutation causes congenital myopathy with fibre-type disproportion.
Lorenzoni PJ, Filla L, Dal-Prá Ducci R, Fustes OJH, Raquel do Vale Pascoal Rodrigues P, Arndt RC, Suemi Kamoi Kay C, Werneck LC, Scola RH. Lorenzoni PJ, et al. Neurol Sci. 2025 Feb;46(2):1019-1022. doi: 10.1007/s10072-024-07810-3. Epub 2024 Oct 31. Neurol Sci. 2025. PMID: 39477909
MELAS: clinical features, muscle biopsy and molecular genetics.
Lorenzoni PJ, Scola RH, Kay CS, Arndt RC, Freund AA, Bruck I, Santos ML, Werneck LC. Lorenzoni PJ, et al. Among authors: arndt rc. Arq Neuropsiquiatr. 2009 Sep;67(3A):668-76. doi: 10.1590/s0004-282x2009000400018. Arq Neuropsiquiatr. 2009. PMID: 19722047 Free article.
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