The mutations and VNTRs in the phenylalanine hydroxylase gene of phenylketonuria in St Petersburg.
Autor: | Baranovskaya S; Petersburg Institute of Nuclear Physics, Gatchina, Russia., Shevtsov S, Maksimova S, Kuzmin A, Schwartz E |
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Jazyk: | angličtina |
Zdroj: | Journal of inherited metabolic disease [J Inherit Metab Dis] 1996; Vol. 19 (5), pp. 705. |
DOI: | 10.1007/BF01799853 |
Databáze: | MEDLINE |
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