Co-Authors
This is a "connection" page, showing publications co-authored by FERNANDO SCAGLIA and ALISON BERTUCH.
Connection Strength
0.584
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Multi-generational mitochondrial complex V deficiency due to the recurrent ATP5F1A c.620G>A?(p.Arg207His) pathogenic variant: A novel family and a review of the literature. Mol Genet Metab. 2026 Sep-Oct; 149(1-2):110207.
Score: 0.246
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Expansion of the clinical phenotype of GALE deficiency. Am J Med Genet A. 2021 10; 185(10):3118-3121.
Score: 0.173
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Hematologic presentation and the role of untargeted metabolomics analysis in monitoring treatment for riboflavin transporter deficiency. Am J Med Genet A. 2020 11; 182(11):2781-2787.
Score: 0.164