Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation
- 30 November 2008
- journal article
- Published by Elsevier BV in Genomics
- Vol. 92 (5), 273-278
- https://doi.org/10.1016/j.ygeno.2008.06.009
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Disentangling the roots of inherited hair disordersNature Genetics, 2008
- G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growthNature Genetics, 2008
- P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicleDevelopment, 2008
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital HypotrichosisJournal of Investigative Dermatology, 2006
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp ErosionsJournal of Investigative Dermatology, 2006
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive HypotrichosisJournal of Investigative Dermatology, 2006
- Desmoglein 4 in Hair Follicle Differentiation and Epidermal AdhesionCell, 2003
- Opposing effects on TSC‐22 expression by BMP and receptor tyrosine kinase signals in the developing feather tractDevelopmental Dynamics, 2001
- Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherinNature Genetics, 2001
- A Gene for Hypotrichosis Simplex of the Scalp Maps to Chromosome 6p21.3American Journal of Human Genetics, 2000