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.

2) Laminopathy.org

3) EURORDIS-Rare Diseases Europe

4) Rare Disease Day

5) ClinGen – Clinical Genome Resource

6) AlphaFold Protein Structure Database

7) How the 3D organization of DNA controls cell identity (Video)

8) Pathogenic LMNA variants disrupt cardiac lamina-chromatin interactions and de-repress alternative fate genes (paper)

Other foundations:

1) L-CMD Research Foundation

2) Fundación Andrés Marcio, Niños Contra La Laminopatía (Spanish website / foundation) – Facebook link

Countries:

The Netherlands

Hartenbank

Netherlands Heart Institute

UK

Cardiomyopathy UK

Australia

Cardiomyopathy Association Of Australia

Germany

ARVC-Selbsthilfe

Italy

AICARM Onlus

Italian Network for Laminopathies

Spain

SAMS

US

DCM Foundation

ChildrensCardiomyopathyFoundation

Hypertrophic Cardiomyopathy Association

Partners:

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