Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia.

author
dbId 70681
displayName Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia.
journal Hum Mol Genet
modified [InstanceEdit:6783922] D'Eustachio, Peter, 2015-06-17
pages 1411-5
pubMedIdentifier 9700195
schemaClass LiteratureReference
title Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia.
url http://www.ncbi.nlm.nih.gov/pubmed/9700195
volume 7
year 1998
Cite Us!