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LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy.
Mull A, Kim G, Holaska JM. LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy. Muscle Nerve. 2015 Feb; 51(2):222-8.
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PubMed
subject areas
Animals
Body Mass Index
Body Weight
Disease Models, Animal
Echocardiography
Gene Expression Regulation
Heart Diseases
Humans
LIM Domain Proteins
Mice
Mice, Inbred C57BL
Mice, Knockout
Mitogen-Activated Protein Kinases
Muscle Contraction
Muscle, Skeletal
Muscular Dystrophy, Emery-Dreifuss
Neuromuscular Junction Diseases
Phenotype
Signal Transduction
Transcription Factors
authors with profiles
James Holaska
Gene H. Kim
LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy.