Co-Authors
This is a "connection" page, showing publications co-authored by FERNANDO SCAGLIA and RONIT MAROM.
Connection Strength
0.281
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Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency. Am J Med Genet A. 2026 Apr 05.
Score: 0.247
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Milder clinical and biochemical phenotypes associated with the c.482G>A (p.Arg161Gln) pathogenic variant in cobalamin C disease: Implications for management and screening. Mol Genet Metab. 2017 09; 122(1-2):60-66.
Score: 0.034