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Article

Etiological investigations in apparent type 2 diabetes: when to search for lamin A/C mutations?

Diabetes & metabolism - 1 Dec 2005

Donadille B, Lascols O, Capeau J, Vigouroux C

Abstract excerpt

Prevalence of diabetes is increasing worldwide in epidemic proportions. Its appropriate clinical management requires a careful etiological diagnosis. Laminopathies recently emerged as clinically heterogeneous genetic disorders due to mutations in lamins or lamin-associated proteins, which are components of the nuclear envelope. Laminopathies regroup at least eight distinct diseases, belonging to the groups of...

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Source

Identifiers

PMID: 16357800
DOI: 10.1016/s1262-3636(07)70227-6

Genes

LMNA

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.

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Etiological investigations in apparent type 2 diabetes: when to search for lamin A/C mutations?PMID 16357800Read ↗

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Type A insulin resistance syndrome revealing a novel lamin A mutation.Semantic proximity Read ↗

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Association between nuclear lamin A/C R482Q mutation and partial lipodystrophy with hyperinsulinemia, dyslipidemia, hypertension, and diabetes.Semantic proximity Read ↗

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