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Children with suspected hereditary spastic paraplegia clearly benefit from whole exome analysis

Dana Safka Brozkova1, Jaroslava Paulasova Schwabova2,3, Emilie Vyhnalkova2,4

  • 1Neurogenetic Laboratory, Department of Paediatric Neurology, Second Faculty of Medicine, Charles University, Motol and Homolka University Hospital, Prague, Czechia.

Human Genomics
|February 26, 2026
PubMed
Abstract

No abstract available in PubMed .

Keywords:
ChildExome sequencingHereditaryNervous system diseasesSpastic paraplegia

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