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Vanishing white matter disease, a rare leukodystrophy with mutation in the EIF2B5 gene.

Authors :
SINKÓ, Gabriella
TOMPA, Márton
KISS, Zsuzsanna
KÁLMÁN, Bernadette
Source :
Clinical Neuroscience / Ideggyógyászati Szemle; 5/30/2024, Vol. 77 Issue 5/6, p207-211, 5p
Publication Year :
2024

Abstract

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Details

Language :
English
ISSN :
00191442
Volume :
77
Issue :
5/6
Database :
Complementary Index
Journal :
Clinical Neuroscience / Ideggyógyászati Szemle
Publication Type :
Academic Journal
Accession number :
177583442
Full Text :
https://doi.org/10.18071/isz.77.0207