Publication | Closed Access
Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy
56
Citations
27
References
2000
Year
Mitochondrial MyopathySevere CourseMendelian DisorderGenetic DisorderGeneticsBecker Muscular DystrophyPathologyMolecular GeneticsDisease Gene IdentificationMedicine
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