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3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces.

Sarah Catharina GrünertJörn Oliver Sass
Published in: Orphanet journal of rare diseases (2020)
This comprehensive data analysis provides a systematic overview on all published cases with HMGCLD including a list of all known HMGCL mutations.
Keyphrases
  • data analysis
  • randomized controlled trial
  • systematic review