Associated Papers
Implications of CLSPN Variants in Cellular Function and Susceptibility to Cancer.
Azenha D et al.
Cancers, 2020
Validation of CZECANCA (CZEch CAncer paNel for Clinical Application) for targeted NGS-based analysis of hereditary cancer syndromes.
Soukupova J et al.
Plos One, 2018
29649263 (PubMed )
Supplement: pone.0195761.s005.xlsx › S5
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A8-A06Q-01A.domain
Germline alterations in the CLSPN gene in breast cancer families.
Erkko H et al.
Cancer Letters, 2008
Mutational analysis of thirty-two double-strand DNA break repair genes in breast and pancreatic cancers.
Wang X et al.
Cancer Research, 2008
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