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MFSD8 Mutation Causing Neuronal Ceroid Lipofuscinosis Type 7 in a Bangladeshi Patient: A Rare Case Report and Review of Literature
by Bithi Debnath, Ramesh Chandra Nath, Seikh Azimul Hoque and Narayan Chandra Saha
American Journal of Medical Case Reports. 2020, 8(12), 508-511. DOI: 10.12691/ajmcr-8-12-21
Pub. Date: September 25, 2020Views: 7380Downloads: 8125
Neuronal ceroid lipofuscinosis (NCL) MFSD8 CLN7 Variant late-infantile NCL visual loss exome sequencing
Abstract Full Text PDF (380 KB) Full Text HTML Full Text ePUB (1410 KB)
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