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Publications by Caitlin A. Fitzgerald
An Exon 53 Frameshift Mutation in CUBN Abrogates Cubam Function and Causes Imerslund-Gräsbeck Syndrome in Dogs
Molecular Genetics and Metabolism
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Related publications
Compound Heterozygosity of a Novel Exon 3 Frameshift (p.R357P Fs*24) Mutation and Y486D Mutation in Exon 5 of the UGT1A1 Gene in a Thai Infant With Crigler-Najjar Syndrome Type 2
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
A Synonymous Mutation in SPINK5 Exon 11 Causes Netherton Syndrome by Altering Exonic Splicing Regulatory Elements
Journal of Human Genetics
Genetics
Frameshift Mutation
A -Defensin Mutation Causes Black Coat Color in Domestic Dogs
Science
Multidisciplinary
Philosophy of Science
History
A De Novo Heterozygous Frameshift Mutation Identified in BCL11B Causes Neurodevelopmental Disorder by Whole Exome Sequencing
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Mutation in Exon 13 of the TCOF1 Gene in Patient With Treacher Collins Syndrome
Acta Fytotechnica et Zootechnica
Animal Science
Zoology
Agronomy
Crop Science
Food Science
Mutation of an A-Kinase-Anchoring Protein Causes Long-Qt Syndrome
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Gain-Of-Function Mutation in theGRIK2gene Causes Neurodevelopmental Deficits
Neurology: Genetics
Neurology
Genetics
A Mutation in MT-TW Causes a tRNA Processing Defect and Reduced Mitochondrial Function in a Family With Leigh Syndrome
Mitochondrion
Molecular Medicine
Cell Biology
Molecular Biology
