Wessagowit, Vesarat

Clinical and molecular significance of splice site mutations in the plakophilin 1 gene in patients with ectodermal dysplasia-skin fragility syndrome. [electronic resource] - Acta dermato-venereologica 2005 - 386-8 p. digital

Publication Type: Comment; Editorial

0001-5555

10.1080/00015550510011763 doi


Ectodermal Dysplasia--genetics
Heterozygote
Humans
Mutation
Plakophilins--genetics
RNA Splice Sites--genetics