| Name | disease |
| Summary | Mechanism page covering IVNS1ABP mutation discovered in Nature Communications (2026) — a unique progeroid syndrome with selective neurological deficits caused by actin cytoskeleton disruption, asymmetric cell division, cytokinesis-linked DNA damage, and cellular senescence. |
| Related Diseases | Cognitive Impairment, Bipolar, Pain |
| Linked Hypotheses | 25 hypotheses |