Elsayed, Liena E. O.; Mohammed, Inaam N.; Hamed, Ahlam A. A.; Elseed, Maha A.; Salih, Mustafa A. M.; Yahia, Ashraf; Siddig, Rayan A.; Amin, Mutaz; Koko, Mahmoud; Elbashir, Mustafa I.; Ibrahim, Muntaser E.; Brice, Alexis; Ahmed, Ammar E.; Stevanin, Giovanni
(BMC Medical Genetics, 2018)
Background:
Infantile neuroaxonal dystrophy (INAD) is a rare hereditary neurological disorder caused by mutations
in
PLA2G6
. The disease commonly affects children below 3 years of age and presents with delay in motor ...