Associated Papers
Whole-exome sequencing identifies novel pathogenic mutations and putative phenotype-influencing variants in Polish limb-girdle muscular dystrophy patients.
Fichna JP et al.
Human Genomics, 2018
29970176 (PubMed )
Supplement: 40246_2018_167_MOESM3_ESM.xlsx › skeletal_muscle
The contribution of rare and common variants in 30 genes to risk nicotine dependence.
Yang J et al.
Molecular Psychiatry, 2015
Identification of Deleterious SNPs and Their Effects on Structural Level in CHRNA3 Gene.
Chandramohan V et al.
Biochemical Genetics, 2015
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