[Analysis of GFM1 gene mutations in a family with combined oxidative phosphorylation deficiency 1].
Article in Journal of Zhejiang University (Medical Sciences) (October 2020)
The most recent citing publications are shown below. View all 4 publications that cite this research output on Dimensions.
Clinical and molecular findings in a family expressing a novel heterozygous variant of the G elongation factor mitochondrial 1 gene
Article in Experimental and Therapeutic Medicine (October 2020)
Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits
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