WNT10A gene is the second molecular candidate in a cohort of young Italian subjects with ectodermal derivative impairment (EDI).
Clinical genetics 2017 Oct .
Guazzarotti L, Tadini G, Mancini G E, Sani I, Pisanelli S, Galderisi F, D'Auria E, Secondi R, Bottero A, Zuccotti G
Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements.
Journal of human genetics 2016 Jun .
Wohlfart Sigrun, Hammersen Johanna, Schneider Ho