Whole exome sequencing in Serbian patients with hereditary spastic paraplegia-Reference-Cited by-同舟云学术

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Whole exome sequencing in Serbian patients with hereditary spastic paraplegia

Published:2024-03-19 Issue:3 Volume:25 Page:165-177
ISSN:1364-6753
Container-title:Neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Brankovic Marija^ORCID,Ivanovic Vukan,Basta Ivana,Khang Rin,Lee Eugene,Stevic Zorica,Ralic Branislav,Tubic Radoje,Seo GoHun,Markovic Vladana,Bozovic Ivo,Svetel Marina,Marjanovic Ana,Veselinovic Nikola,Mesaros Sarlota,Jankovic Milena,Savic-Pavicevic Dusanka,Jovin Zita,Novakovic Ivana,Lee Hane,Peric Stojan

Funder

Yonsei University

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s10048-024-00755-x.pdf

Reference59 articles.

1. de Souza PVS, de Rezende Pinto WBV, de Rezende Batistella GN, Bortholin T, Oliveira ASB (2017) Hereditary Spastic Paraplegia: Clinical and Genetic Hallmarks. Cerebellum 16(2):525–551

2. Ruano L, Melo C, Silva MC, Coutinho P (2014) The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies. Neuroepidemiology 42(3):174–183

3. Schüle R, Wiethoff S, Martus P et al (2016) Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients. Ann Neurol 79(4):646–658

4. Murala S, Nagarajan E, Bollu PC (2021) Hereditary spastic paraplegia. Neurol Sci 42(3):883–894

5. Darios F, Coarelli G, Durr A (2022) Genetics in hereditary spastic paraplegias: Essential but not enough. Curr Opin Neurobiol 72:8–14

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