Associated Papers
Whole-genome sequencing in clinically diagnosed Charcot-Marie-Tooth disease undiagnosed by whole-exome sequencing.
Kim YG et al.
Brain Communications, 2023
37180992 (PubMed )
Supplement: fcad139_supplementary_data.zip › Supplementary_Table_1_and_Supplementary_References.docx
Screening for SH3TC2 variants in Charcot-Marie-Tooth disease in a cohort of Chinese patients.
Sun B et al.
Acta Neurologica Belgica, 2022
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