A novel insertion mutation of CDSN responsible for hypotrichosis simplex of scalp in a Chinese family.

Authors :: Huang H
Sun J
Fu L
Wu J
Guo H
Yang C
Zheng X
Tang H
Sun L
Zhang X
Source :: Clinical and experimental dermatology [Clin Exp Dermatol] 2018 Aug; Vol. 43 (6), pp. 722-723. Date of Electronic Publication: 2018 May 24.
Publication Year :: 2018

Subjects :: China epidemiology
Genetic Variation genetics
Humans
Hypotrichosis genetics
Hypotrichosis pathology
Intercellular Signaling Peptides and Proteins
Male
Middle Aged
Mutation
Pedigree
Scalp pathology
Alopecia genetics
Glycoproteins genetics
Hypotrichosis congenital
Mutagenesis, Insertional genetics
Scalp abnormalities

Full Text Access

Tools