Retinitis Pigmentosa Associated with Bardet-Biedl Syndrome with BBS9 Gene Mutation in a Korean Patient

Lignende værker

• Structural Characterization of Bardet-Biedl Syndrome 9 Protein (BBS9)
  af: Knockenhauer, Kevin E., et al.
  Udgivet: (2015)
• Identification of Compound Heterozygous Mutations in the BBS7 Gene in a Korean Family with Bardet-Biedl Syndrome
  af: Shin, Seok Joon, et al.
  Udgivet: (2015)
• Knockdown of Bardet-Biedl Syndrome Gene BBS9/PTHB1 Leads to Cilia Defects
  af: Veleri, Shobi, et al.
  Udgivet: (2012)
• Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases
  af: Kim, Min Seok, et al.
  Udgivet: (2019)
• Bardet-Biedl Syndrome in Rhesus Macaques: A Nonhuman Primate Model of Retinitis Pigmentosa
  af: Peterson, Samuel M., et al.
  Udgivet: (2019)