1) Laminopathies Support Group (mutations in the LMNA Gene) (Facebook group)
2) A Study of ARRY-371797 (PF-07265803) in Patients With Symptomatic Dilated Cardiomyopathy Due to a Lamin A/C Gene Mutation (REALM-DCM) – Pfizer (information also available in Dutch)
3) REALM-DCM: A clinical trial for adults with symptomatic dilated cardiomyopathy (DCM) due to an LMNA gene mutation.
4) Universal Mutation Database – LMNA
5) LMNA Biobank
General information
1) PubMed® comprises more than 32 million citations for biomedical literature from MEDLINE, life science journals, and online books.
3) EURORDIS-Rare Diseases Europe
5) ClinGen – Clinical Genome Resource
6) AlphaFold Protein Structure Database
7) How the 3D organization of DNA controls cell identity (Video)
9) New Strategies for the Treatment of Dilated Cardiomyopathy
10) Striated muscle laminopathies – natural history and clinical trial readiness
11) Laminopathies’ Treatments Systematic Review: A Contribution Towards a ‘Treatabolome’
12) National Protocol for Diagnosis and Care (PNDS) Laminopathies with cardiac presentation (French)
Get connected:
Other foundations:
2) Fundación Andrés Marcio, Niños Contra La Laminopatía (Spanish website / foundation) – Facebook link
Countries:
The Netherlands
Heart Tissue Bank / Hartenbank
UK
Australia
Cardiomyopathy Association Of Australia
Germany
France
Italy
Italian Network for Laminopathies
Spain
US
ChildrensCardiomyopathyFoundation
Hypertrophic Cardiomyopathy Association
Partners:





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