Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes.

Authors:
Elert-Dobkowska E; Stepniak I; Krysa W; Ziora-Jakutowicz K; Rakowicz M and 5 more

Journal:
Neurogenetics

Publication Year: 2019

DOI:
10.1007/s10048-019-00565-6

PMCID:
PMC6411833

PMID:
30778698

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Journal Information

Full Title: Neurogenetics

Abbreviation: Neurogenetics

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Neurology

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

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Evidence found in paper:

"Funding information This study was financed by Operational Programme Innovative Economy, Activity 1.1.2 (UDA-POIG.01.01.02-14-051/09-00) and the Ministry of Education and Science internal programme: “Designing the diagnostic tool for genetic analysis of the hereditary spastic paraplegia using Next Generation Sequencing – NGS.”"

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Last Updated: Aug 05, 2025