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Partial characterization and three-dimensional-structural localization of eight mutations in exon 7 of the human phenylalanine hydroxylase gene associated with phenylketonuria

✍ Scribed by Elisa Bjørgo; Per M. Knappskog; Aurora Martinez; Raymond C. Stevens; Torgeir Flatmark


Book ID
114429374
Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
587 KB
Volume
257
Category
Article
ISSN
1432-1327

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