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Rare Gene Intelligence Dispatch
Join our monthly digest for genomic breakthroughs, clinical trial alerts, patient narratives, and policy updates curated for global rare disease communities.
What to Expect
- • Spotlight dossiers on emerging rare diseases and variant annotations.
- • Clinical trial trackers with enrollment windows and inclusion criteria.
- • Patient and caregiver stories highlighting culturally responsive care.
- • Funding calls, policy developments, and collaborative project openings.
Archive Highlights
August 2025
CRISPR base editing insights for CDKL5 deficiency, tele-genetics models in East Africa, and new funding streams for lysosomal storage disorders.
July 2025
AI-driven diagnosis toolkits, patient mentorship networks, and proteomic biomarker breakthroughs.
June 2025
Global newborn screening expansion, partnership playbook for cross-border registries, and advocacy storytelling templates.