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BACKGROUND Familial Idiopathic Basal Ganglia Calcification (IBGC) is a rare neurodegenerative disorder which is usually transmitted as an autosomal dominant trait. IBGC is genetically heterogeneous(More)
OBJECTIVES Current study was the first to report a consanguineous Iranian pedigree with ABCD1 mutation. METHODS Targeted molecular analysis was initially performed in three affected individuals in(More)