Trichothiodystrophy: Update on the sulfur deficient brittle hair syndromes

Journal of the American Academy of Dermatology

Volumn 44, Issue 6, 2001, Pages 891-924

  Itin, Peter H ^a,b,c   Sarasin, Alain ^a,b,c   Pittelkow, Mark R ^a,b,c  

^a UNIVERSITY OF BASEL   (Switzerland)

^b Institute de Recherche sur le Cancer   (France)

^c MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MATRIX PROTEIN; RNA; SULFUR; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR IIH; UNCLASSIFIED DRUG;

AUTOSOMAL RECESSIVE DISORDER; BRITTLE HAIR SYNDROME; CANCER RISK; CLINICAL FEATURE; COCKAYNE SYNDROME; DIAGNOSTIC PROCEDURE; DISEASE CLASSIFICATION; DNA REPAIR; GENE MUTATION; GENOTYPE; GROWTH RETARDATION; HAIR DISEASE; HUMAN; NEUROLOGIC DISEASE; NONHUMAN; PATHOGENESIS; PHENOTYPE; PHOTOSENSITIVITY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVIEW; RNA SYNTHESIS; SKIN CANCER; TRICHOTHIODYSTROPHY; ULTRAVIOLET RADIATION; XERODERMA PIGMENTOSUM;

EID: 0035010089     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1067/mjd.2001.114294     Document Type: Article

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