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Open AccessCase Report

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: 7666 Downloads: 8567Like: 4

Neuronal ceroid lipofuscinosis (NCL) MFSD8 CLN7 Variant late-infantile NCL visual loss exome sequencing

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