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Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuria

✍ Scribed by A.J. Schneider; Sterling D. Garrard

Book ID: 118534873
Publisher: Elsevier Science
Year: 1966
Tongue: English
Weight: 963 KB
Volume: 68
Category: Article
ISSN: 1097-6833
DOI: 10.1016/s0022-3476(66)80442-0

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