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A mutation in the X-linked Emery–Dreifuss muscular dystrophy gene in a patient affected with conduction cardiomyopathy
by
Vohanka, Stanislav
,
Vytopil, Michal
,
Bednarik, Josef
,
Lukas, Zdenek
,
Kadanka, Zdenek
,
Schildberger, Jiri
,
Ricotti, Roberta
,
Bione, Silvia
,
Toniolo, Daniela
Published in
Neuromuscular disorders : NMD
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Neuromuscular Disorders : Nmd
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Adult
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Cardiomyopathies - Genetics
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Cardiomyopathies - Physiopathology
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Clinical Neurology
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Conduction Cardiomyopathy
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Emery-Dreifuss Muscular Dystrophy
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Emery–Dreifuss Muscular Dystrophy
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Genetic Linkage
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Heart Conduction System - Physiopathology
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Humans
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Life Sciences & Biomedicine
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Male
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Membrane Proteins - Deficiency
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Muscle, Skeletal - Metabolism
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Muscle, Skeletal - Physiopathology
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Muscular Dystrophy, Emery-Dreifuss - Genetics
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Muscular Dystrophy, Emery-Dreifuss - Metabolism
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Muscular Dystrophy, Emery-Dreifuss - Physiopathology
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Mutation
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Mutations
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Sciencedirect Freedom Collection
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