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

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Bibliographic Details
Main Authors:	Jacquet, H, Berthelot, J, Bonnemains, C, Simard, G, Saugier-Veber, P, Raux, G, Campion, D, Bonneau, D, Frebourg, T
Format:	Artigo
Language:	Inglês
Published:	BMJ Group 2003
Subjects:	Online Mutation Report
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC1735267/ https://ncbi.nlm.nih.gov/pubmed/12525555 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.40.1.e7
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