A Novel Spontaneous Mutation of the SOX10 Gene Associated with Waardenburg Syndrome Type II

Những quyển sách tương tự

• Waardenburg syndrome type II in a Chinese pedigree caused by frameshift mutation in the SOX10 gene
  Bằng: Li, Li, et al.
  Được phát hành: (2021)
• Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome and SOX10 Mutations
  Bằng: Elmaleh-Bergès, M., et al.
  Được phát hành: (2013)
• Novel SOX10 Mutations in Waardenburg Syndrome: Functional Characterization and Genotype-Phenotype Analysis
  Bằng: Thongpradit, Supranee, et al.
  Được phát hành: (2020)
• Kallmann Syndrome Due to Heterozygous Mutation in SOX10 Coexisting With Waardenburg Syndrome Type II: Case Report and Review of Literature
  Bằng: Chen, Kan, et al.
  Được phát hành: (2021)
• Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss
  Bằng: Wang, Xiao-Hui, et al.
  Được phát hành: (2021)