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The genetic spectrum and clinical features of X-linked juvenile retinoschisis in Central China.

Zhenhui LiuJu GuoMeng PanKunpeng XieLiping DuXuemin JinBo Lei
Published in: Ophthalmic genetics (2023)
mutations and associated clinical phenotypes but also provide a basis for mechanistic studies and diagnosis of XLRS.
Keyphrases
  • genome wide
  • copy number
  • dna methylation