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

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Medicine & Life Sciences