Compound heterozygous mutations in two different domains of ALDH18A1 do not affect the amino acid levels in a patient with hereditary spastic paraplegia

Maria Steenhof*, Maria Kibæk, Martin J. Larsen, Mette Christensen, Allan Meldgaard Lund, Klaus Brusgaard, Jens Michael Hertz

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

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Medicine & Life Sciences