Smahi, Asma

Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases

Cluzeau, C., Hadj-Rabia, S., Jambou, M., Mansour, S., Guigue, P., Masmoudi, S., Bal, E., Chassaing, N., Vincent, M.-C., Viot, G., et al. (2011) · Human Mutation

dental development and anomaliesGenetic and rare skin diseases.

Cited by 311

Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus

Bal, E., Baala, L., Cluzeau, C., El Kerch, F., Ouldim, K., Hadj-Rabia, S., Bodemer, C., Munnich, A., Courtois, G., Sefiani, A., et al. (2007) · Human Mutation

dental development and anomaliesGenetic and rare skin diseases.

Cited by 100

Clinical and histologic features of incontinentia pigmenti in adults with nuclear factor-κB essential modulator gene mutations

Hadj-Rabia, S., Rimella, A., Smahi, A., Fraitag, S., Hamel-Teillac, D., Bonnefont, J.-P., de Prost, Y., & Bodemer, C. (2011) · Journal of the American Academy of Dermatology

Genetic and rare skin diseases.Skin and Cellular Biology Research

Cited by 57