A missense mutation in the type II hair keratin hHb3 is associated with monilethrix

Bibliographic Details

Published in:	Journal of medical genetics 2005-03, Vol.42 (3), p.e19-e19
Main Authors:	van Steensel, M A M, Steijlen, P M, Bladergroen, R S, Vermeer, M, van Geel, M
Format:	Article
Language:	eng
Subjects:	Adolescent Alopecia - genetics Child Child, Preschool DNA Mutational Analysis Female Genetic Testing Genotype hair loss Heterozygote hHb3 Humans Keratins - chemistry Keratins - genetics Keratins, Hair-Specific Keratins, Type II monilethrix Mutation, Missense Online Mutation Report Polymorphism, Genetic type II hair keratin
Online Access:	Get full text
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