DeMille D
No ORCID on file
· 2 papers in corpus
· active 2024
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Frequent coauthors
- Elloumi HZ 2
- Ambrosini G 2
- Chrast J 2
- Duncan L 2
- Bayrak-Toydemir P 2
- Bassani S 2
- Brusco A 2
- Arikka H 2
- Butler KM 2
- Flores-Gallegos L 2
2024
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles.
BackgroundWe previously described the KINSSHIP syndrome, an autosomal dominant disorder associated with intellectual disability (ID), mesomelic dysplasia and horseshoe kidney, caused by de novo variants in the degron of AFF3. Mouse knock-in…
2024
Background We previously described the KINSSHIP syndrome, an autosomal dominant disorder associated with intellectual disability (ID), mesomelic dysplasia and horseshoe kidney,caused by de novo variants in the degron of AFF3. Mouse knock-in…