Skip to main navigation Skip to search Skip to main content

A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorption

Research output: Contribution to journalArticlepeer-review

28 Citations (Scopus)

Fingerprint

Dive into the research topics of 'A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorption'. Together they form a unique fingerprint.
Sort by

Biochemistry, Genetics and Molecular Biology