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
Jazyk: angličtina
Zdroj: Journal of inherited metabolic disease [J Inherit Metab Dis] 1996; Vol. 19 (5), pp. 705.
DOI: 10.1007/BF01799853
Databáze: MEDLINE