Cargando…
Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population
INTRODUCTION: Childhood acute lymphoblastic leukaemia (ALL) is a complex disease caused by a combination of genetic susceptibility and environmental exposure. Previous genome-wide association studies have reported several single nucleotide polymorphisms (SNPs) associated with the incidence of ALL. S...
Autores principales: | Kreile, Madara, Piekuse, Linda, Rots, Dmitrijs, Dobele, Zane, Kovalova, Zhanna, Lace, Baiba |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889682/ https://www.ncbi.nlm.nih.gov/pubmed/27279837 http://dx.doi.org/10.5114/aoms.2016.59920 |
Ejemplares similares
-
Association of ARID5B Genetic Variants with Risk of Childhood B Cell Precursor Acute Lymphoblastic Leukaemia in Latvia
por: Kreile, Madara, et al.
Publicado: (2018) -
Genetic variation spectrum in ATP7B gene identified in Latvian patients with Wilson disease
por: Zarina, Agnese, et al.
Publicado: (2017) -
Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome
por: Gailite, Linda, et al.
Publicado: (2018) -
UGT1A1 Variants c.864+5G>T and c.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene Assays
por: Gailite, Linda, et al.
Publicado: (2020) -
X-Linked Lymphoproliferative Disease in Latvia: A Report of Two Clinically Distinct Cases
por: Nokalna, Ieva, et al.
Publicado: (2020)