1 Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD [期刊论文]
来源:Frontiers in Genetics , 2023
作者:Carlo Caltagirone;Valerio Caputo;Luca Colantoni;等
关键词:FSHD;exome;...
使用许可:Unknown
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