M. Saj

Variants of the Lamin A / C ( LMNA ) Gene in Non-Valvular Atrial Fibrillation Patients A Possible Pathogenic Role of the Thr 528 Met Mutation

R. Płoski, H. Szwed, R. Dąbrowski, 2012 .

LMNA mutations in Polish patients with dilated cardiomyopathy: prevalence, clinical characteristics, and in vitro studies

J. Korewicki, R. Płoski, F. Tesson, 2013, BMC Medical Genetics.

Lamin A/C mutations in dilated cardiomyopathy.

R. Płoski, F. Tesson, Z. Bilińska, 2014, Cardiology journal.

A new c.1621 C>G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis): genotype–phenotype correlation

R. Płoski, F. Tesson, Z. Bilińska, 2011, Journal of Human Genetics.

Variants of the lamin A/C (LMNA) gene in non-valvular atrial fibrillation patients: a possible pathogenic role of the Thr528Met mutation.

R. Płoski, H. Szwed, R. Dąbrowski, 2012, Molecular diagnosis & therapy.

Variants of the Lamin A/C (LMNA) Gene in Non-Valvular Atrial Fibrillation Patients

R. Płoski, H. Szwed, R. Dąbrowski, 2012, Molecular Diagnosis & Therapy.