Hyperprolinaemia in patients with deleti... [J Inherit Metab Dis. 2000] - PubMed

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The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene. [J Med Genet. 2003]
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A human homologue of the Drosophila melanogaster sluggish-A (proline oxidase) gene maps to 22q11.2, and is a candidate gene for type-I hyperprolinaemia. [Hum Genet. 1997]
A human homologue of the Drosophila melanogaster sluggish-A (proline oxidase) gene maps to 22q11.2, and is a candidate gene for type-I hyperprolinaemia.
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Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome.
Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome.
J Inherit Metab Dis. 2000 Dec ;23(8):847-8.

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