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Neurogenetics|August 9, 2005
The Gem interacting protein (GMIP) gene is associated with major depressive disorderKazuyuki Tadokoro, Ryota Hashimoto, Masahiko Tatsumi, et al.
Neurogenetics|January 17, 2004
Analysis of sequence variability of the bovine prion protein gene (PRNP) in German cattle breedsPetra Sander, Henning Hamann, Ina Pfeiffer, et al.
Neurogenetics|October 2, 2004
A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signsMaria Spadaro, Simona Ursu, Frank Lehmann-Horn, et al.
Neurogenetics|September 30, 2004
Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer diseaseKristin K Nicodemus, Judith E Stenger, Donald E Schmechel, et al.
Neurogenetics|December 4, 2003
New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian familiesNacim Louhichi, Chahnez Triki, Susana Quijano-Roy, et al.
Neurogenetics|August 8, 2008
The location of DCX mutations predicts malformation severity in X-linked lissencephalyPierre-Louis Leger, Isabelle Souville, Nathalie Boddaert, et al.
Neurogenetics|September 24, 2008
Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9-2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP)Thilo Herzfeld, Nicole Wolf, Pia Winter, et al.
Neurogenetics|October 16, 2008
Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutationLena Skoglund, RoseMarie Brundin, Tommie Olofsson, et al.
Neurogenetics|June 28, 2018
Clinical and genetic study of Tunisian families with genetic generalized epilepsy: contribution of CACNA1H and MAST4 genesZied Landoulsi, Fatma Laatar, Eric Noé, et al.
Neurogenetics|July 5, 2018
R106C TFG variant causes infantile neuroaxonal dystrophy "plus" syndromeA Catania, R Battini, T Pippucci, et al.
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