A novel TRPS1 mutation in a Moroccan family with Tricho-rhino-phalangeal syndrome type III: case report

por Smaili, W., Elalaoui, S. Chafai, Meier, S., Zerkaoui, M., Sefiani, A., Heinimann, K.
Publicado 2017

Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: a case report

por Berrani, H., Meskini, T., Zerkaoui, M., Merhni, H., Ettair, S., Sefiani, A., Mouane, N.
Publicado 2018

Clinical and molecular report of novel GALC mutations in Moroccan patient with Krabbe disease: case report

por Zerkaoui, M., Ratbi, I., Castellotti, B., Gellera, C., Lyahyai, J., Kriouile, Y., Sefiani, A.
Publicado 2015