Methods of treatment, genetic screening, and disease models for heart conditions associated with RBM20 deficiency
US-12391989-B2 · Aug 19, 2025 · US
This patent family groups 2 related publications across US. Members often share priority claims or equivalent filings in different countries.
| Field | Value |
|---|---|
| Family ID | 70464483 |
| Family type | — |
| Earliest priority | Oct 30, 2018 |
| First filing country | US |
| Member publications | 2 |
| Countries | US |
| Representative publication | US12391989B2 — Methods of treatment, genetic screening, and disease models for heart conditions associated with RBM20 deficiency |
Best representative member for this family based on priority and filing country.
US12391989B2 — Methods of treatment, genetic screening, and disease models for heart conditions associated with RBM20 deficiency (published Aug 19, 2025)
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