X-linked heterozygous mutations in ARR3 cause female-limited early onset high myopia

Lignende værker

• Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopia
  af: Li, Jiali, et al.
  Udgivet: (2016)
• Novel RS1 mutations associated with X-linked juvenile retinoschisis
  af: YI, JUNHUI, et al.
  Udgivet: (2012)
• Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism
  af: Fang, Shaohua, et al.
  Udgivet: (2008)
• Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese
  af: Ji, Yanli, et al.
  Udgivet: (2010)
• CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projection
  af: Ouyang, Jiamin, et al.
  Udgivet: (2019)