Melatonin alterations and brain acetylcholine lesions in sleep disorders in Cockayne syndrome

Abstract Background: Cockayne syndrome (CS) is a genetic disorder caused by deficient nucleotide excision repair. Patients with CS exhibit progeroid features, developmental delay, and various neurological disorders; they are also known to suffer from sleep problems, which have never been investigate...

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Bibliographic Details
Published inBrain & development (Tokyo. 1979) Vol. 36; no. 10; pp. 907 - 913
Main Authors Okoshi, Yumi, Tanuma, Naoyuki, Miyata, Rie, Hayashi, Masaharu
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.11.2014
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