W. Jdioui

Clinical and molecular findings in three Moroccan families with distal renal tubular acidosis and deafness: Report of a novel mutation of ATP6V1B1 gene.

A. Sefiani, I. Ratbi, K. Soulami, 2016, Current research in translational medicine.

Post-mortem diagnosis of Pompe disease by exome sequencing in a Moroccan family: a case report

A. Sefiani, I. Ratbi, M. Taoudi, 2018, Journal of Medical Case Reports.

A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report

L. Raymond, J. Lyahyai, A. Sefiani, 2018, BMC Medical Genetics.