A new missense mutation in PLA2G6 gene among a family with infantile neuroaxonal dystrophy INAD
By: Jibril, Ula; Uebe, Steffen; Reuter, Miriam…[et al.]. Egyptian Pediatric Association Gazette. Vol. 64, no. 4 (Dec. 2016), pp.171-176, 6 p.
Subjects: Brain; Case studies; Children; Diseases; Mutation