Associated Papers
Mutational insights and in silico characterization of NEK family kinases in OSCC patients from the Pakistani population.
Nawab F et al.
Frontiers in Bioinformatics, 2025
41716219 (PubMed )
Supplement: Table1.docx
Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis.
Ruf WP et al.
Brain Communications, 2023
37223130 (PubMed )
Supplement: fcad152_supplementary_data.pdf
NEK1 Variants in a Cohort of Italian Patients With Amyotrophic Lateral Sclerosis.
Riva N et al.
Frontiers in Neuroscience, 2022
35495032 (PubMed )
Supplement: Data_Sheet_1.docx
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