Mutations in the Δ 1 -pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia

Author: Geraghty M.T.  

Publisher: Oxford University Press

E-ISSN: 0964-6906|7|9|1411-1415

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.7, Iss.9, 1998-09, pp. : 1411-1415

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