Co-Authors
This is a "connection" page, showing publications co-authored by FERNANDO SCAGLIA and KEVIN GLINTON.
Connection Strength
0.268
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Multiple mitochondrial dysfunctions syndrome 1: An unusual cause of developmental pulmonary hypertension. Am J Med Genet A. 2020 04; 182(4):755-761.
Score: 0.158
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Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency. Am J Med Genet A. 2026 Aug; 200(8):1814-1820.
Score: 0.061
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Natural history of TANGO2 deficiency disorder: Baseline assessment of 73 patients. Genet Med. 2023 04; 25(4):100352.
Score: 0.048