Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families.

Issa, Yasmin A

Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families. [electronic resource] - European journal of human genetics : EJHG 10 2016 - 1430-5 p. digital

Publication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.

1476-5438

10.1038/ejhg.2016.29 doi


Adolescent
Anodontia--diagnosis
Child
Chromosomes, Human, Pair 22--genetics
Ectodermal Dysplasia--diagnosis
Exome
Female
Genes, Recessive
Humans
Male
Membrane Proteins--genetics
Mutation
Pedigree
Syndrome
Wnt Signaling Pathway