Co-Authors
This is a "connection" page, showing publications co-authored by LISA EMRICK and EMILY WASKOW.
Connection Strength
0.278
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Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndrome. Am J Med Genet A. 2025 01; 197(1):e63845.
Score: 0.216
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COX14 Variants Are Associated With Mitochondrial Complex IV Deficiency Nuclear Type 10 (MC4DN10). Am J Med Genet A. 2026 Aug 26.
Score: 0.062