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Neurogenetics|February 17, 2016
Recessive mutations of TMC1 associated with moderate to severe hearing lossAyesha Imtiaz, Azra Maqsood, Atteeq U Rehman, et al.Neurogenetics|August 17, 2019
VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesisMoran Hausman-Kedem, Shay Ben-Shachar, Shay Menascu, et al.Neurogenetics|December 23, 2003
Friedreich ataxia-update on pathogenesis and possible therapiesMax Voncken, Panos Ioannou, Martin B DelatyckiNeurogenetics|October 14, 2004
Alternative splicing in the N-terminus of Alzheimer's presenilin 1Wiep Scheper, Rob Zwart, Frank BaasNeurogenetics|May 25, 2004
Private SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) families from TurkeyAndrea M Richter, Riza Koksal Ozgul, Virginie C Poisson, et al.Neurogenetics|November 2, 2004
Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3AAnnette Abel, Nuria Fonknechten, Anne Hofer, et al.Neurogenetics|May 27, 2005
Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosisCarol Dobson-Stone, Antonio Velayos-Baeza, An Jansen, et al.Neurogenetics|December 7, 2007
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohortsChristina L Liquori, Silvana Penco, Judith Gault, et al.Neurogenetics|December 7, 2007
Myotonic dystrophy type 2 in Japan: ancestral origin distinct from Caucasian familiesTsukasa Saito, Yoshinobu Amakusa, Takashi Kimura, et al.Neurogenetics|May 18, 1999
HLA typing in the United Kingdom multiple sclerosis genome screenF Coraddu, S Sawcer, R Feakes, et al.Pageof 96