Published in Eur J Hum Genet on August 13, 2008
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Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis. Neurosciences (Riyadh) (2012) 0.75
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Direct sequencing of FAH gene in Pakistani tyrosinemia type 1 families reveals a novel mutation. J Pediatr Endocrinol Metab (2016) 0.75