Corrigendum: Whole-exome sequencing identifies a novel CPT2 mutation in a pedigree with gout

مواد مشابهة

• Corrigendum: Whole-exome sequencing identifies a novel CPT2 mutation in a pedigree with gout
  حسب: Yong Guo, وآخرون
  منشور في: (2022-08-01)
• Identification of pathogenic mutations for a Wolfram syndrome pedigree by whole exome sequencing and analysis of its clinical characteristics
  حسب: MENG Xiangyu, وآخرون
  منشور في: (2023-07-01)
• Case report: Whole exome sequencing and genome-wide methylation profiling of Czech dysplasia in a Chinese pedigree
  حسب: Mengfei Zhao, وآخرون
  منشور في: (2023-11-01)
• Whole-exome sequencing identifies a CD38 variant in a Chinese family with hodgkin’s lymphoma
  حسب: Xi Chen, وآخرون
  منشور في: (2026-01-01)
• Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families
  حسب: Yingjie Zhou, وآخرون
  منشور في: (2020-07-01)