Compound pathogenic mutation in the USH2A gene in Chinese RP families detected by whole-exome sequencing

Những quyển sách tương tự

• Novel USH2A compound heterozygous mutations cause RP/USH2 in a Chinese family
  Bằng: Liu, Xiaowen, et al.
  Được phát hành: (2010)
• The genomic mutation spectrums of breast fibroadenomas in Chinese population by whole exome sequencing analysis
  Bằng: Xie, Shang‐Nao, et al.
  Được phát hành: (2019)
• Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa
  Bằng: Méndez-Vidal, Cristina, et al.
  Được phát hành: (2013)
• Targeted exome sequencing identified novel USH2A mutations in Usher syndrome families.
  Bằng: Xiu-Feng Huang, et al.
  Được phát hành: (2013-01-01)
• Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families
  Bằng: Huang, Xiu-Feng, et al.
  Được phát hành: (2013)