An Early Diagnostic Clue for COL18A1- and LAMA1-Associated Diseases: High Myopia With Alopecia Areata in the Cranial Midline

Lignende værker

• Phenotypic characterization of patients with early-onset high myopia due to mutations in COL2A1 or COL11A1: Why not Stickler syndrome?
  af: Zhou, Lin, et al.
  Udgivet: (2018)
• An evaluation of OPTC and EPYC as candidate genes for high myopia
  af: Wang, Panfeng, et al.
  Udgivet: (2009)
• Sequence variations of GRM6 in patients with high myopia
  af: Xu, Xiaoyu, et al.
  Udgivet: (2009)
• An Ophthalmic Targeted Exome Sequencing Panel as a Powerful Tool to Identify Causative Mutations in Patients Suspected of Hereditary Eye Diseases
  af: Wang, Panfeng, et al.
  Udgivet: (2019)
• Replication study of significant single nucleotide polymorphisms associated with myopia from two genome-wide association studies
  af: Wang, Qin, et al.
  Udgivet: (2011)