Rogaev_1999_Lancet_354_1097

Reference

Title : Total hypotrichosis: genetic form of alopecia not linked to hairless gene - Rogaev_1999_Lancet_354_1097
Author(s) : Rogaev EI , Zinchenko RA , Dvoryachikov G , Sherbatich T , Ginter EK
Ref : Lancet , 354 :1097 , 1999
Abstract :

We describe a hereditary form of alopecia in an aboriginal Finno-Ugric population. Linkage and mutation analyses of 21 families showed that the disorder was not linked to the hairless gene on chromosome 8. This implies that an isolated hairless defect caused by a single gene is a genetically heterogeneous disorder in human populations.

PubMedSearch : Rogaev_1999_Lancet_354_1097
PubMedID: 10509509
Gene_locus related to this paper: human-LIPH

Related information

Mutation Delexon4_human-LIPH
Gene_locus human-LIPH
Disease Hypotrichosis

Citations formats

Rogaev EI, Zinchenko RA, Dvoryachikov G, Sherbatich T, Ginter EK (1999)
Total hypotrichosis: genetic form of alopecia not linked to hairless gene
Lancet 354 :1097

Rogaev EI, Zinchenko RA, Dvoryachikov G, Sherbatich T, Ginter EK (1999)
Lancet 354 :1097