Publication | Closed Access

A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum

Mendelian DisorderMental ImpairmentGenetic DisorderGeneticsNew LocusClinical GeneticsTunisian FamilyMolecular GeneticsMedical GeneticsNeurologyDisease Gene IdentificationNeuropathologyMedicineNeurogenetics