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Article

Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity.

Archives of neurology - 1 Mar 2008

Boukhris Amir, Stevanin Giovanni, Feki Imed, Denis Elodie, Elleuch Nizar, Miladi Mohamed Imed, Truchetto Jérémy, Denora Paola, Belal Samir, Mhiri Chokri, Brice Alexis

Abstract excerpt

OBJECTIVE: To perform a clinical and genetic study of Tunisian families with autosomal recessive (AR) hereditary spastic paraplegia with thin corpus callosum (HSP-TCC). DESIGN: Linkage studies and mutation screening. SETTING: Reference Center for Neurogenetics in South and Center Tunisia. PARTICIPANTS: Seventy-three subjects from 33 "apparently" unrelated Tunisian families with AR HSP. MAIN OUTCOME MEASURES:...

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Source

Identifiers

PMID: 18332254
DOI: 10.1001/archneur.65.3.393

Genes

SPG11

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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