Detalhe da pesquisa
1.
Mutations in the cholesterol transporter gene ABCA5 are associated with excessive hair overgrowth.
PLoS Genet
; 10(5): e1004333, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-24831815
2.
Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation.
Genomics
; 92(5): 273-8, 2008 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-18692127
3.
Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions.
J Invest Dermatol
; 126(6): 1286-91, 2006 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-16543896