Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
Copyright policy )Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
Key Points Inherited genetic variation increases risk to developing multiple myeloma through predisposition to MGUS. Loci identified that increase risk of developing MGUS include 2p23.3, 3p22.1, 3q26.2, 6p21.33, 7p15.3, 17p11.2, and 22q13.1.
- Lund University Sweden
- German Center for Neurodegenerative Diseases Germany
- Essen University Hospital Germany
- LMU Klinikum Germany
- Leeds Teaching Hospitals NHS Trust United Kingdom
epidemiology [Multiple Myeloma], Male, Genotype, Medizin, Germany/epidemiology, epidemiology [Germany], epidemiology [Monoclonal Gammopathy of Undetermined Significance], Monoclonal Gammopathy of Undetermined Significance, Polymorphism, Single Nucleotide, Germany, Humans, genetics [Multiple Myeloma], Genetic Predisposition to Disease, Genetic Association Studies, Aged, Aged, 80 and over, Middle Aged, genetics [Monoclonal Gammopathy of Undetermined Significance], Disease Progression, pathology [Monoclonal Gammopathy of Undetermined Significance], Multiple Myeloma/epidemiology, Female, aged, 80 and over, Multiple Myeloma, Monoclonal Gammopathy of Undetermined Significance/epidemiology, ddc: ddc:610
epidemiology [Multiple Myeloma], Male, Genotype, Medizin, Germany/epidemiology, epidemiology [Germany], epidemiology [Monoclonal Gammopathy of Undetermined Significance], Monoclonal Gammopathy of Undetermined Significance, Polymorphism, Single Nucleotide, Germany, Humans, genetics [Multiple Myeloma], Genetic Predisposition to Disease, Genetic Association Studies, Aged, Aged, 80 and over, Middle Aged, genetics [Monoclonal Gammopathy of Undetermined Significance], Disease Progression, pathology [Monoclonal Gammopathy of Undetermined Significance], Multiple Myeloma/epidemiology, Female, aged, 80 and over, Multiple Myeloma, Monoclonal Gammopathy of Undetermined Significance/epidemiology, ddc: ddc:610
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