Publication | Open Access

Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype

Huntington-like PhenotypeMendelian DisorderGenetic DisorderMedicineGeneticsGenetic EpidemiologyMolecular BiologyMolecular GeneticsFtl GenesGenetic FactorDisease Gene IdentificationNeurodegenerationPortuguese Patients