Co-Authors
This is a "connection" page, showing publications co-authored by LISA EMRICK and DARYL SCOTT.
Connection Strength
0.294
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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. 2024 Aug 21; e63845.
Score: 0.245
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COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. Am J Hum Genet. 2021 09 02; 108(9):1710-1724.
Score: 0.050