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A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree.

Jingliang ChengJiewen FuQi ZhouXiaohong XiangChunli WeiLisha YangShangyi FuMd Asaduzzaman KhanHongbin LvJunjiang Fu
Published in: Journal of cellular and molecular medicine (2019)
Keyphrases
  • copy number
  • genome wide
  • genome wide identification
  • transcription factor
  • genome wide analysis