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Expanding the clinical and genetic spectrum of Heimler syndrome.

Feng-Juan GaoFang-Yuan HuPing XuYu-He QiJian-Kang LiYong-Jin ZhangFang ChenQing ChangFang SongSi-Mai ShenGe-Zhi XuFeng-Juan Gao
Published in: Orphanet journal of rare diseases (2019)
Next-generation sequencing is important for the diagnosis of HS. This study expands the clinical and genetic spectrum of HS, and provides additional insights into genotype-phenotype correlations, which is vital for accurate clinical practice, genetic counseling, and pathogenesis studies.
Keyphrases
  • copy number
  • genome wide
  • clinical practice
  • high resolution
  • gene expression
  • mass spectrometry