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Article

Adult-onset neurological degeneration in a patient with Cockayne syndrome and a null mutation in the CSB gene.

The Journal of investigative dermatology - 1 Jun 2008

Hashimoto Satoru, Suga Tomohiro, Kudo Erina, Ihn Hironobu, Uchino Makoto, Tateishi Satoshi

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PMID: 18185538
DOI: 10.1038/sj.jid.5701210

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Related research

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Adult-onset neurological degeneration in a patient with Cockayne syndrome and a null mutation in the CSB gene.PMID 18185538Read ↗

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Cockayne syndrome type A: novel mutations in eight typical patients.Semantic proximity Read ↗

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A C. elegans model for neurodegeneration in Cockayne syndrome.Semantic proximity Read ↗

The identification and analysis of mutation in the Cockayne Syndrome B geneSemantic proximity Read ↗

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Cockayne syndrome: review of 140 cases.Semantic proximity Read ↗

A comprehensive description of the severity groups in Cockayne syndrome.Semantic proximity Read ↗

Progressive demyelinating neuropathy correlates with clinical severity in Cockayne syndrome.Semantic proximity Read ↗

[The metabolic and molecular bases of Cockayne syndrome].Semantic proximity Read ↗

Cockayne syndrome pathogenesis: lessons from mouse models.Semantic proximity Read ↗

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