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Brain & Development|October 25, 2018
Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrumA Iodice, M Carecchio, G Zorzi, et al.Annals of Human Genetics|September 1, 1996
Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansionsM Frontali, G Sabbadini, A Novelletto, et al.American Journal of Human Genetics|February 17, 2001
Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2S Guida, F Trettel, S Pagnutti, et al.Annals of Human Genetics|October 11, 2001
A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean areaP Malaspina, M Tsopanomichalou, T Duman, et al.Pageof 3