Associated Papers
Multi-Center National Study of Genotype-Phenotype Correlation and Clinical Characteristics in Children and Young Adults with Friedreich's Ataxia from Serbia.
Kovacevic G et al.
Biomedicines, 2025
Genetic and Phenotypic Variability in Siblings With Friedreich Ataxia.
Eshaghi K et al.
Neurology. Genetics, 2025
HAPLN3 p.T34A contributes to incomplete penetrance of moyamoya disease in Chinese carrying RNF213 p.R4810K.
Xu J et al.
European Journal of Neurology, 2024
39315749 (PubMed )
Supplement: ENE-31-e16473-s001.xlsx › Table_S2
Lack of association between polymorphisms in the SIRT6 gene and longevity in a Chinese population.
Lin R et al.
Molecular and Cellular Probes, 2016
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