Lmna H222P homozygous and heterozygous mutant models of Emery-Dreifuss muscular dystrophy: hearts - - GEO DataSets - NCBI

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Full record GDS2746

Lmna H222P homozygous and heterozygous mutant models of Emery-Dreifuss muscular dystrophy: hearts

Analysis of hearts of A-type lamin Lmna H222P homo-/heterozygous mutants. LMNA mutations lead to autosomal dominant and recessive Emery-Dreifuss muscular dystrophy which is characterized by dilated cardiomyopathy. Results provide insight into the role of LMNA in the development of cardiomyopathy.

Organism:: Mus musculus

Type:: Expression profiling by array, count, 3 genotype/variation sets

Platform:: GPL1261
Series:: GSE8000
21 Samples

Download data: CEL

DataSet

Accession:: GDS2746

ID:: 2746

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Lmna H222P homozygous and heterozygous mutant models of Emery-Dreifuss muscular ...
Lmna H222P homozygous and heterozygous mutant models of Emery-Dreifuss muscular dystrophy: hearts
Accession: GDS2746

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