Mutations in the Δ1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia

Michael T. Geraghty, D. Vaughn, A. J. Nicholson, Wei Wen Lin, Gerardo Jimenez-Sanchez, Cassandra Obie, M. P. Flynn, David Valle, Chien An A. Hu

Research output: Contribution to journalArticlepeer-review

71 Scopus citations

Fingerprint

Dive into the research topics of 'Mutations in the Δ1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia'. Together they form a unique fingerprint.

Medicine & Life Sciences