A novel GJB6 missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basis.

Authors	H N Baris, A Zlotogorski, G Peretz-Amit, V Doviner, M Shohat, H Reznik-Wolf, E Pras
Journal	The British journal of dermatology (Br J Dermatol) Vol. 159 Issue 6 Pg. 1373-6 (Dec 2008) ISSN: 1365-2133 [Electronic] England
PMID	18717672 (Publication Type: Case Reports, Journal Article)
Chemical References	Connexins
Topics	Connexins (genetics) Ectodermal Dysplasia (genetics, pathology) Female Humans Infant Male Mutation, Missense Polymerase Chain Reaction Young Adult

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.

Realize the full power of the drug-disease research graph!