Associated Papers
Novel Polymorphisms and Genetic Features of the Prion Protein Gene (PRNP) in Cats, Hosts of Feline Spongiform Encephalopathy.
Kim HH et al.
Genes, 2020
A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.
Tran C et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2013
A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy.
Hicks D et al.
Brain : a Journal of Neurology, 2011
Allelic variants of DYX1C1 are not associated with dyslexia in India.
Saviour P et al.
Indian Journal of Human Genetics, 2008
No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy.
Bellini G et al.
Journal of Molecular Neuroscience : Mn, 2005
Highly conserved prion protein sequences in random bred cats with three novel synonymous PRNP gene variants.
Güven C et al.
Topics in Companion Animal Medicine, 0
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