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Publications by Irene Marcos
NOVEL Intronic CAPN3 Roma Mutation Alters Splicing Causing RNA Mediated Decay
Annals of Clinical and Translational Neurology
Neuroscience
Neurology
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Alternative Splicing and Nonsense-Mediated RNA Decay Contribute to the Regulation of SHOX Expression
PLoS ONE
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In Vitro Antisense Therapeutics for a Deep Intronic Mutation Causing Neurofibromatosis Type 2
European Journal of Human Genetics
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RNA Secondary Structure Mediated by Alu Insertion as a Novel Disease-Causing Mechanism
Familial Wilms Tumour Resulting From WT1 Mutation: Intronic Polymorphism Causing Artefactual Constitutional Homozygosity
Journal of Medical Genetics
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a Novel Intronic Mutation in MTM1 Detected by RNA Analysis in a Case of X-Linked Myotubular Myopathy
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Novel CDHR1 Mutation Causing Cone Rod Dystrophy
Acta Ophthalmologica
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Novel Mutation in KCNQ2 Causing Ohtahara Syndrome
Annals of Child Neurology
Novel C8ORF37 Mutation Causing Cone Rod Dystrophy
Acta Ophthalmologica
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The Coupling of Alternative Splicing and Nonsense-Mediated mRNA Decay
Advances in Experimental Medicine and Biology
Biochemistry
Medicine
Genetics
Molecular Biology