Mutations in LAMA2 and CAPN3 genes associated with genetic and phenotypic heterogeneities within a single consanguineous family involving both congenital and progressive muscular dystrophies

Authors: Salem, I.H., Kamoun, F., Louhichi, N., Rouis, S., Mziou, M., Fendri-Kriaa, N., Makni-Ayadi, F., Triki, C., Fakhfakh, F.

Source: BIOSCIENCE REPORTS. 31(2):125-135

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN289162986&indx=1&recIds=ETOCRN289162986

The First Genome-Wide Scan in a Tunisian Family With Generalized Epilepsy With Febrile Seizure Plus (GEFS+)

Authors: Fendri-Kriaa, N., Louhichi, N., Mkaouar-Rebai, E., Chabchoub, G., Kammoun, F., Salem, I.H., Rebai, A., Triki, C., Fakhfakh, F.

Source: JOURNAL OF CHILD NEUROLOGY. 25(11):1362-1368

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN282239278&indx=1&recIds=ETOCRN282239278