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A rare case of intermediate phenotype Niemann-Pick disease with a rare pathogenic variant of 1624C>T in SMPD1 gene.

Deepthi KrishnaPradeep Kumar GunasekaranJanki KumariVeena LaxmiLokesh SainiKuldeep Singh
Published in: Journal of neurosciences in rural practice (2022)
Keyphrases
  • rare case
  • copy number
  • genome wide
  • genome wide identification
  • gene expression
  • dna methylation
  • transcription factor