Progeroid features in a patient with Malouf syndrome due to a rare LMNA variant: a case report and review of the literature. [PDF]
Pekmezci A, Gumus AA, Korkmaz OP.
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Genetically Confirmed Familial Case of Nonsyndromic Cardiac Progeria Caused by the <i>LMNA</i> p.Asp300Asn Variant with Presumed Gonadal Mosaicism: Phenotypic Comparison with Previously Reported Patients. [PDF]
Nuzhnaya E +5 more
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Telomere shortening in laminopathic dilated cardiomyopathy. [PDF]
Chang ACY +11 more
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Pathogenic LMNA variant identified in a family with dilated cardiomyopathy and arrhythmias highlights cascade screening importance. [PDF]
Zhou L, Li J.
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When Off-Target <i>Is</i> the Target: Treating Noncardiomyocytes in Cardiac Laminopathy. [PDF]
Kirk JA.
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Muscular dystrophy-associated lamin variants disrupt cellular organization through a nucleolar-ribosomal axis. [PDF]
Ding X +4 more
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Lamins' role in osteosarcoma. [PDF]
Bagnato G, Peruzzi B.
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Clustering cell nuclei on microgrooves for disease diagnosis using deep learning. [PDF]
Roellinger B +5 more
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Recognizing red flags in genetic cardiomyopathy: the importance of genetic testing. [PDF]
Gerges S, Chouairi S, Naoufal R.
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