Xeroderma pigmentosum: Its overlap with trichothiodystrophy, cockayne syndrome and other progeroid syndromes

Advances in Experimental Medicine and Biology

Volumn 637, Issue , 2008, Pages 128-137

  Lambert, W Clark ^a   Gagna, Claude E ^a   Lambert, Muriel W ^b  

^a RUTGERS NEW JERSEY MEDICAL SCHOOL   (United States)

^b New York Law Institute   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA DIRECTED RNA POLYMERASE; RNA POLYMERASE II; XERODERMA PIGMENTOSUM GROUP D PROTEIN;

ATAXIA; BRAIN CALCIFICATION; BRAIN VENTRICLE; CARDIOVASCULAR DISEASE; CATARACT; CLINICAL FEATURE; COCKAYNE SYNDROME; DEVELOPMENTAL DISORDER; DISEASE CLASSIFICATION; DNA RECOMBINATION; DWARFISM; EXCISION REPAIR; FAMILIAL DISEASE; GENE MUTATION; GENODERMATOSIS; GROWTH DISORDER; HUMAN; HUMAN CELL CULTURE; HYPERREFLEXIA; HYPERSENSITIVITY; MENTAL DEFICIENCY; MICROCEPHALY; MICROPHTHALMIA; MORTALITY; NERVE CONDUCTION; NERVE DEGENERATION; OPTIC NERVE ATROPHY; PATHOPHYSIOLOGY; PERCEPTION DEAFNESS; PHENOTYPE; PHOTOSENSITIVITY; PRIORITY JOURNAL; PROGERIA; RETINA PIGMENT DEGENERATION; REVIEW; RNA SYNTHESIS; RNA TRANSCRIPTION; SEXUAL DEVELOPMENT; SUN EXPOSURE; SUNBURN; SUNLIGHT; TELANGIECTASIA; TRANSCRIPTION INITIATION; TRICHOTHIODYSTROPHY; ULTRAVIOLET IRRADIATION; ULTRAVIOLET SENSITIVITY SYNDROME; XERODERMA PIGMENTOSUM; XEROSIS; GENETICS;

COCKAYNE SYNDROME; HUMANS; PROGERIA; TRICHOTHIODYSTROPHY SYNDROMES; XERODERMA PIGMENTOSUM;

EID: 60549084198     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-0-387-09599-8_14     Document Type: Review

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