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Neurological phenotype in Fabry disease: case series with GLA missense variant c.749 A > C (p.Gln250Pro).

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Title:	Neurological phenotype in Fabry disease: case series with GLA missense variant c.749 A > C (p.Gln250Pro).
Authors:	Stamenković, Marija^1,2 (AUTHOR) marija.stamenkovic@mf.uns.ac.rs, Slavić, Danijel¹ (AUTHOR) danijel.slavic@mf.uns.ac.rs, Rajić, Sonja^1,2 (AUTHOR) sonja.rajic@mf.uns.ac.rs, Hajder, Dragica^1,2 (AUTHOR) dragica.hajder@mf.uns.ac.rs, Popović, Sanela^1,2 (AUTHOR) sanela.popovic@mf.uns.ac.rs, Jovićević, Predrag^1,3 (AUTHOR) predrag.jovicevic@mf.uns.ac.rs, Jovićević, Maša^1,4 (AUTHOR) masa.jovic@mf.uns.ac.rs, Ćelić, Dejan^1,5 (AUTHOR) dejan.celic@mf.uns.ac.rs, Živanović, Željko^1,2 (AUTHOR) zeljko.zivanovic@mf.uns.ac.rs
Source:	Egyptian Journal of Neurology, Psychiatry & Neurosurgery. 6/15/2026, Vol. 62 Issue 1, p1-6. 6p.
Database:	Academic Search Ultimate
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Description
ISSN:	11101083
DOI:	10.1186/s41983-026-01192-3