Patient with actin aggregate myopathy and not formerly identified ACTA1 mutation is heterozygous for the Gly15Arg mutation of ACTA1, which has previously been associated with actinopathy
- PMID: 16948949
- DOI: 10.1177/08830738060210060103
Patient with actin aggregate myopathy and not formerly identified ACTA1 mutation is heterozygous for the Gly15Arg mutation of ACTA1, which has previously been associated with actinopathy
Comment on
-
Actin-related myopathy without any missense mutation in the ACTA1 gene.J Child Neurol. 2004 Feb;19(2):149-53. doi: 10.1177/08830738040190021201. J Child Neurol. 2004. PMID: 15072110
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
