DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Elsayed LEO, Mohammed IN, Hamed AAA. et al.
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family.
BMC Med Genet 2018;
19 (01) 72-76
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