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Pediatrics and Rare Diseases Group
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variants underlying X-linked intellectual disability disrupt protein function via distinct mechanisms.
Life science alliance Mar, 2024 | Pubmed ID: 38182161
Sanford Research
Intisar Koch1,
Matthew J. Schellenberg2,
Francisco Bustos1,3
1Pediatrics and Rare Diseases Group, Sanford Research,
2Department of Biochemistry and Molecular Biology, Mayo Clinic,
3Department of Pediatrics, Sanford School of Medicine, University of South Dakota
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