Associated Papers
Genetics of childhood tuberculosis: A scoping review.
Pinheiro Mascarenhas MA et al.
Paediatric Respiratory Reviews, 2025
Genetic mutations in lymphocytic variant of hypereosinophilic syndrome: study of five siblings.
Walkenhorst M et al.
Frontiers in Medicine, 2025
41488087 (PubMed )
Supplement: Table_1.xlsx › Data
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
Chen W et al.
Frontiers in Neurology, 2022
36619910 (PubMed )
Supplement: Data_Sheet_6.ZIP › case2-C › 3.________ › CA2275B________.____Exonic_Variants.xlsx › sheet1
Complement C5a receptor gene 450 C/T polymorphism in renal transplant recipients: association of the CT genotype with graft outcome.
Günesacar R et al.
Tissue Antigens, 2015
Association between CCL2 haplotypes and knee osteoarthritis.
Hulin-Curtis SL et al.
International Journal of Immunogenetics, 2013
Gene variants of monocyte chemoattractant protein 1 and components of metabolic syndrome in KORA S4, Augsburg.
Sedlmeier EM et al.
European Journal of Endocrinology, 2007
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