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Article

LINC complex alterations in DMD and EDMD/CMT fibroblasts.

European journal of cell biology - 1 Aug 2012

Taranum Surayya, Vaylann Eva, Meinke Peter, Abraham Sabu, Yang Liu, Neumann Sascha, Karakesisoglou Iakowos, Wehnert Manfred, Noegel Angelika A

Abstract excerpt

Emery-Dreifuss muscular dystrophy (EDMD) is a late onset-disease characterized by skeletal muscle wasting and heart defects with associated risk of sudden death. The autosomal dominant form of the disease is caused by mutations in the LMNA gene encoding LaminA and C, the X-linked form results from mutations in the gene encoding the inner nuclear membrane protein Emerin (STA). Both Emerin and LaminA/C interact...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 22555292
DOI: 10.1016/j.ejcb.2012.03.003
PMCID: PMC3778752

Genes

DMD
LMNA
SUN1
SUN2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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