Total hypotrichosis: Genetic form of alopecia not linked to hairless gene

Lancet

Volumn 354, Issue 9184, 1999, Pages 1097-1098

  Rogaev, E I ^a   Zinchenko, R A ^b   Dvoryachikov, G ^a   Sherbatich, T ^a   Ginter, E K ^b  

^a MENTAL HEALTH RESEARCH CENTER   (Russian Federation)

^b RESEARCH CENTRE FOR MEDICAL GENETICS   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

ABORIGINE; ALOPECIA; ARTICLE; CHROMOSOME 8; GENE MUTATION; GENETIC LINKAGE; HUMAN; HYPOTRICHOSIS; PRIORITY JOURNAL;

EID: 0033604101     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(99)02816-0     Document Type: Note

References (5)

1. Cantu J.M., Sanchez-Corona J., Gonzales-Mendoza A.et al. Autosomal recessive inheritance of atrichia congenita. Clin Genet. 17:1980;209-212.
2. Vogt B.R., Traupe H., Hamm H. Congenital atrichia with nail dystrophy, abnormal facies, and retarded psychomotor development in two siblings: a new autosomal recessive syndrome? Pediatr Dermatol. 5:1988;236-242.
3. Ahmad W., Haque M., Brancolini V.et al. Alopecia universalis associated with a mutation in the human hairless gene. Science. 279:1998;720-724.
4. Frank J., Pignata C., Panteleev A.A.et al. Exposing the human nude phenotype. Nature. 398:1999;473-474.
5. Ahmad W., Zlotogorski A., Panteleev A.A.et al. Genomic organisation of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family. Genomics. 56:1999;141-148.