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Article

The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene.

Journal of medical genetics - 1 Jan 2003

Jacquet H, Berthelot J, Bonnemains C, Simard G, Saugier-Veber P, Raux G, Campion D, Bonneau D, Frebourg T

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Topics

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Share to Amino Acid Metabolism, Inborn Errors
Share to Chromosome Deletion
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Share to Chromosomes, Human, Pair 22

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 12525555
DOI: 10.1136/jmg.40.1.e7
PMCID: PMC1735267

Genes

PRODH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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