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Cockayne syndrome type II

Cockayne syndrome, type B
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Cockayne syndrome type II" returned 0 free, full-text research articles. First 0 results:
Cockayne syndrome type II in a Druze isolate in Northern Israel in association with an insertion mutation in ERCC6.
Last Updated: Nov 16, 2017

Cockayne syndrome (CS) (OMIM #133540) is a rare autosomal recessive disease characterized by severe growth and developmental retardation, progressive neurological dysfunction and symptoms of premature aging. The underlying cause of the disease is a defect in transcription-coupled ...

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