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Myofibrillar myopathy phenotype due to recessive mutations in MEGF10
Myofibrillar myopathy phenotype due to recessive mutations in MEGF10
2017
E. Harris
Ana Töpf
Judith N Hudson
Rita Barresi
K. Bushby
Hanns Lochmüller
Volker Straub
Keywords:
Genetics
Biology
Diabetes mellitus
Phenotype
Myofibrillar myopathy
MEGF10
Dominance (genetics)
Correction
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