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Publications by Christine Hough
A Novel Type 2A Von Willebrand Factor Mutation Located at the Last Nucleotide of Exon 26 (3538G>A) Causes Skipping of 2 Nonadjacent Exons
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Aberrant Splicing and Premature Termination of Transcription of the FVIII Gene as a Cause of Severe Canine Hemophilia A: Similarities With the Intron 22 Inversion Mutation in Human Hemophilia
Thrombosis and Haemostasis
Hematology
Related publications
Identification and Functional Analysis of a Novel Von Willebrand Factor Mutation in a Family With Type 2A Von Willebrand Disease
PLoS ONE
Multidisciplinary
The Silent Mutation Nucleotide 744 G → A, Lys172Lys, in Exon 6 of BRCA2 Results in Exon Skipping
Breast Cancer Research and Treatment
Cancer Research
Oncology
An ANK1 IVS3-2A>C Mutation Causes Exon 4 Skipping in Two Patients From a Chinese Family With Hereditary Spherocytosis
Oncotarget
Oncology
Functional Analysis of a Type IIB Von Willebrand Disease Missense Mutation: Increased Binding of Large Von Willebrand Factor Multimers to Platelets.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
GT to AT Transition at a Splice Donor Site Causes Skipping of the Preceding Exon in Phenylketonuria
Nucleic Acids Research
Genetics
Von Willebrand Factor and Angiopoietin-2
Critical Care Medicine
Critical Care
Intensive Care Medicine
Splicing Analysis Disclosed a Determinant Single Nucleotide for Exon Skipping Caused by a Novel Intraexonic Four-Nucleotide Deletion in the Dystrophin Gene
Journal of Medical Genetics
Genetics
Clearance of Von Willebrand Factor
Journal of Thrombosis and Haemostasis
Medicine
Hematology
A T+6 to C+6 Mutation in the Donor Splice Site of COL3A1 IVS7 Causes Exon Skipping and Results in Ehlers-Danlos Syndrome Type IV.
Journal of Medical Genetics
Genetics
