Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia

Br J Dermatol. 2008 Mar;158(3):614-7. doi: 10.1111/j.1365-2133.2007.08383.x. Epub 2007 Dec 11.

Authors

J Zhao¹, R Hua, X Zhao, Y Meng, Y Ao, Q Liu, D Shang, M Sun, W H-Y Lo, X Zhang

Affiliation

¹ Department of Medical Genetics and National Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

PMID: 18076698
DOI: 10.1111/j.1365-2133.2007.08383.x

No abstract available

MeSH terms

Amino Acid Sequence
Chromosomes, Human, X / genetics*
Ectodermal Dysplasia / genetics*
Ectodysplasins / genetics*
Genetic Linkage
Humans
Hypohidrosis / genetics*
Male
Mutation / genetics*
Pedigree
Polymerase Chain Reaction / methods

Substances

EDA protein, human
Ectodysplasins