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Clinical and genetic spectrum of primary ciliary dyskinesia in Chinese patients: a systematic review.

Bo PengYong-Hua GaoJia-Qi XieXiao-Wen HeCong-Cong WangJin-Fu XuGuo-Jun Zhang
Published in: Orphanet journal of rare diseases (2022)
PROSPERO; No.: CRD42021257804; URL: www.crd.york.ac.uk/prospero/.
Keyphrases
  • genome wide
  • cross sectional
  • copy number
  • gene expression
  • dna methylation