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Article

Muscle MRI findings in patients with an apparently exclusive cardiac phenotype due to a novel LMNA gene mutation.

Neuromuscular disorders : NMD - 1 Apr 2008

Carboni Nicola, Mura Marco, Marrosu Giovanni, Cocco Eleonora, Ahmad Mohammad, Solla Elisabetta, Mateddu Anna, Maioli Maria Antonietta, Marini Stefano, Nissardi Vincenzo, Frau Jessica, Mallarini Giorgio, Mercuro Giuseppe, Marrosu Maria Giovanna

Abstract excerpt

The case of a family in which several members displayed conduction defects inherited as a dominant trait is reported. The proband was a young woman with a 1st degree atrio-ventricular block and high serum creatine kinase. Several members of the family featured cardiologic symptoms. All adult fami...

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Source

Identifiers

PMID: 18337098
DOI: 10.1016/j.nmd.2008.01.009

Genes

LMNA

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18337098-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Muscle MRI findings in patients with an apparently exclusive cardiac phenotype due to a novel LMNA gene mutation.PMID 18337098Read ↗

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