A case of mitochondrial trifunctional protein deficiency with hadhb variants diagnosed using whole-exome sequencing

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)194-198
Number of pages5
JournalAnnals of Child Neurology
Volume29
Issue number4
DOIs
StatePublished - Oct 2021
Externally publishedYes

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