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Volumn 11, Issue 3, 2006, Pages 150-152

Cockayne's syndrome: A case report. Literature review;Síndrome de Cockayne: Informe de un caso. Revisión de la literatura

Author keywords

CKN1 gene; Cockayne's syndrome; CSA gene; CSB gene; ERCC6 gene; ERCC8 gene; Growth and development retardation; Macrodontia; Oligodontia; Photosensitivity; Premature aging; XPB gene; XPD gene; XPG gene

Indexed keywords

CLINICAL FEATURE; COCKAYNE SYNDROME; DENTAL CARIES; DENTISTRY; DNA REPAIR; ENAMEL HYPOPLASIA; GENE MUTATION; GINGIVITIS; HUMAN; INCISOR; MANDIBLE HYPOPLASIA; MENTAL DEFICIENCY; PHOTOSENSITIVITY; PSYCHOMOTOR PERFORMANCE; REVIEW; VITAL SIGN; X RAY;

EID: 33745102021     PISSN: 16984447     EISSN: 16986946     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (3)

References (12)
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  • 2
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  • 3
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    • Identification of the XPG region that causes the onset of Cockayne syndrome by using Xpg mutant mice generated by the cDNA-mediated knock-in method
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  • 5
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  • 6
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    • Functional crosstalk between hOgg1 and the helicase domain of Cockayne syndrome group B protein
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  • 7
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  • 8
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    • Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome
    • Horibata K, Iwamoto Y, Kuraoka I, Jaspers NG, Kurimasa A, Oshimura M, et al. Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome. Proc Natl Acad Sci U S A 2004;101:15410-5.
    • (2004) Proc Natl Acad Sci U S A , vol.101 , pp. 15410-15415
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  • 9
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    • Lee SK, Yu SL, Prakash L, Prakash S. Requirement of yeast RAD2, a homolog of human XPG gene, for efficient RNA polymerase II transcription, implications for Cockayne syndrome. Cell 2002;109:823-34.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.