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Chromosome 6–Linked Autosomal Recessive Early-Onset Parkinsonism: Linkage in European and Algerian Families, Extension of the Clinical Spectrum, and Evidence of a Small Homozygous Deletion in One Family

Neurodegenerative DiseasesChromosome 6–LinkedMendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyNeurologyDisease Gene IdentificationMedicineAlgerian FamiliesClinical Spectrum