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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.- Sort by
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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 journal › Article › peer-review