Lmna H222P homozygous and heterozygous mutant models of Emery-Dreifuss muscular dystrophy: hearts
Transcriptomics Dataset
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General Information
| Accession | GSE8000 |
| Title | Lmna H222P homozygous and heterozygous mutant models of Emery-Dreifuss muscular dystrophy: hearts |
| Description | 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. |
| Landing Page | https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE8000 |
| Repository | Gene Expression Omnibus |
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