Co-Authors
This is a "connection" page, showing publications co-authored by KEVIN GLINTON and FERNANDO SCAGLIA.
Connection Strength
0.272
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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: 0.161
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Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency. Am J Med Genet A. 2026 Apr 05.
Score: 0.062
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Natural history of TANGO2 deficiency disorder: Baseline assessment of 73 patients. Genet Med. 2023 04; 25(4):100352.
Score: 0.049