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Publications by Catherine Burton
The Exon a (C77G) Mutation Is a Common Cause of Abnormal CD45 Splicing in Humans
Journal of Immunology
Allergy
Immunology
Related publications
A Mutation in Exon 7 of the CFTR Gene Is Common in the Western Part of France.
Journal of Medical Genetics
Genetics
Abnormal Cell Surface Antigen Expression in Individuals With Variant CD45 Splicing and Histiocytosis
Pediatric Research
Child Health
Pediatrics
Perinatology
A 2-Base Insertion in Exon 5 Is a Common Mutation of the TP53 Gene in Dogs With Histiocytic Sarcoma
Journal of Veterinary Medical Science
Veterinary
Alternative Splicing Shapes the Phenotype of a Mutation inBBS8To Cause Nonsyndromic Retinitis Pigmentosa
Molecular and Cellular Biology
Cell Biology
Molecular Biology
A Synonymous Mutation in SPINK5 Exon 11 Causes Netherton Syndrome by Altering Exonic Splicing Regulatory Elements
Journal of Human Genetics
Genetics
Exon Skipping Through the Creation of a Putative Exonic Splicing Silencer as a Consequence of the Cystic Fibrosis Mutation R553X
Journal of Medical Genetics
Genetics
A Naturally Arising Mutation of a Potential Silencer of Exon Splicing in Human Immunodeficiency Virus Type 1 Induces Dominant Aberrant Splicing and Arrests Virus Production.
Journal of Virology
Insect Science
Immunology
Microbiology
Virology
Meningitis Is a Common Cause of Convulsive Status Epilepticus
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Abnormal Hypermethylation of the VDAC2 Promoter Is a Potential Cause of Idiopathic Asthenospermia in Men
Scientific Reports
Multidisciplinary
