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LMNA gene

Discuss publications and research concerning the LMNA gene.

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Related literature

Imaging signatures of high-risk arrhythmogenic genotypes in dilated cardiomyopathy.
LMNA
The p.R249W Mutation in LMNA-Related Congenital Muscular Dystrophy Causes Nuclear Deformities and an Enrichment in Lamin A/C at the Ends of the Nucleus.
LMNA
Somatic mosaicism in ALS and FTD identifies focal mutations associated with widespread degeneration.
LMNA
Familial Generalized and Partial Lipodystrophies Due to Rare Biallelic Variants in LMNA.
LMNA
Restrictive Dermopathy in Neonates.
LMNA
Case Report: Familial partial lipodystrophy, description of novel and ultrarare variants with distinct phenotypic spectrum.
LMNA
Familial partial lipodystrophy type 2 associated with a novel LMNA variant (c.604G>C; p.Glu202Gln): a Colombian family case series.
LMNA
Why and How Are Infants with Hutchinson-Gilford Progeria Syndrome Born Without Severe Manifestations?
LMNA
Unraveling the mysteries of Hutchinson-Gilford progeria syndrome: a comprehensive review of LMNA gene mutations.
LMNA
Liraglutide use in pediatric type 2 familial partial lipodystrophy caused by LMNA mutation: a case report.
LMNA

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