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Publications by Linda Gailite
UGT1A1 Variants C.864+5G>T and C.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene Assays
Frontiers in Genetics
Genetics
Molecular Medicine
The Association of FMR1 Gene (CGG)n Variation With Idiopathic Female Infertility
Archives of Medical Science
Medicine
Related publications
UGT1a1 Gene Mutations in a Tibetan Patient With Crigler-Najjar SyndromeType II - Case Report and Literature Review
Current Trends in Clinical & Medical Imaging
A Novel Pathogenic UGT1A1 Variant in a Sudanese Child With Type I Crigler-Najjar Syndrome
Drug Metabolism and Disposition
Pharmacology
Pharmaceutical Science
Two Unrelated Patients With Rare Crigler-Najjar Syndrome Type I: Two Novel Mutations and a Patient With Loss of Heterozygosity of UGT1A1 Gene
Journal of Zhejiang University: Science B
Genetics
Pharmacology
Molecular Biology
Biochemistry
Veterinary
Medicine
Toxicology
Pharmaceutics
Identification of a Novel Deletion in UDP-glucuronosyltransferase Gene in a Patient With Crigler–Najjar Syndrome Type I
Blood Cells, Molecules, and Diseases
Molecular Medicine
Hematology
Molecular Biology
Cell Biology
The First Case of Crigler-Najjar Syndrome Type-1 in Japan
Acta Hepatologica Japonica
Hepatology
Reduction of Hyperbilirubinemia With Hypericum Extract (St. John's Wort) in a Patient With Crigler-Najjar Syndrome Type II
British Journal of Clinical Pharmacology
Pharmacology
A Novel COL1A1 Gene-Splicing Mutation (C.1875+1G>C) in a Brazilian Patient With Osteogenesis Imperfecta
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
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
ATP-binding Cassette Subfamily A, Member 4 Intronic Variants C.4773+3A>G and C.5461-10t>c Cause Stargardt Disease Due to Defective Splicing
Acta Ophthalmologica
Medicine
Ophthalmology
