Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: A unique patient or a novel metabolic disorder?

Waters, Paula J.; Khashu, Minesh; Lillquist, Yolanda; Senger, Christof; Mattman, André; Demos, Michelle; Setchell, Kenneth D.R.; Rupar, Anthony; Scott, Patrick; Blau, Nenad; Vallance, Hilary

doi:10.1016/j.ymgme.2005.07.032

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Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: A unique patient or a novel metabolic disorder?

Cited by 4 publications

References 13 publications

Neonatal Hemochromatosis and Gestational Alloimmune Liver Disease

Neonatal Hemochromatosis and Gestational Alloimmune Liver Disease

Spectrum of PAH gene mutations and genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Shanxi province

Electrochemical determination of l-phenylalanine at polyaniline modified carbon electrode based on β-cyclodextrin incorporated carbon nanotube composite material and imprinted sol–gel film

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