Associated Papers
Genetic and Phenotypic Spectrum of Amyotrophic Lateral Sclerosis Patients with CCNF Variants from a Large Chinese Cohort.
Zhao B et al.
Molecular Neurobiology, 2023
37171577 (PubMed )
Supplement: 12035_2023_3380_MOESM1_ESM.xlsx › Supplementary_table_4
Effective mismatch repair depends on timely control of PCNA retention on DNA by the Elg1 complex.
Paul Solomon Devakumar LJ et al.
Nucleic Acids Research, 2019
31114918 (PubMed )
Supplement: gkz441_supplemental_files.zip › Supplementary_Tables_2May19TKpm.xlsx › Table_S1
MEN4 and CDKN1B mutations: the latest of the MEN syndromes.
Alrezk R et al.
Endocrine-related Cancer, 2017
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