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Article

Duchenne muscular dystrophy: evidence for somatic reversion of the mutation in man.

Journal of neurology - 1 Dec 1990

Gold R, Meurers B, Reichmann H, Kress W, Müller C R

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 2074453
DOI: 10.1007/BF00314771

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Related research

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Research trail→

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Duchenne muscular dystrophy: evidence for somatic reversion of the mutation in man.PMID 2074453Read ↗

Brief report: reverse mutation in myotonic dystrophy.Semantic proximity Read ↗

Changing clinical concepts of Duchenne muscular dystrophy: molecular genetic diagnosis.Semantic proximity Read ↗

[Spontaneous reversion mutation of Wiskott-Aldrich syndrome pathogenic gene and its clinical implications].Semantic proximity Read ↗

Reversal of a mitochondrial DNA defect in human skeletal muscle.Semantic proximity Read ↗

Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?Semantic proximity Read ↗

[Molecular bases of progressive muscular dystrophy].Semantic proximity Read ↗

The history of a genetic disease: Duchenne muscular dystrophy or Meryon's diseaseSemantic proximity Read ↗

In vivo reversion to normal of inherited mutations in humans.Semantic proximity Read ↗

Genetic study of somatic mosaicism in a patient with myotonic dystrophy type 1: case report.Semantic proximity Read ↗

Duchenne muscular dystrophy in monozygotic twins.Semantic proximity Read ↗

Revertant mosaicism in human genetic disorders.Semantic proximity Read ↗

Revertant Phenomenon in DMD and LGMD2I and Its Therapeutic Implications: A Review of Study Under Mentorship of Terrence Partridge.Semantic proximity Read ↗

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