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Publications by Rita Horvath
Drosophila Studies Support a Role for a Presynaptic Synaptotagmin Mutation in a Human Congenital Myasthenic Syndrome
PLoS ONE
Multidisciplinary
Respiratory-Chain Deficiency Presenting as Diffuse Mesangial Sclerosis With NPHS3 Mutation
Pediatric Nephrology
Child Health
Pediatrics
Perinatology
Nephrology
Late-Onset Sacsinopathy Diagnosed by Exome Sequencing and Comparative Genomic Hybridization
Journal of Neurogenetics
Molecular Neuroscience
Genetics
Cellular
Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal Γ Subunit
American Journal of Human Genetics
Genetics
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