The mutations and VNTRs in the phenylalanine hydroxylase gene of phenylketonuria in St Petersburg-Reference-Cited by-同舟云学术

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The mutations and VNTRs in the phenylalanine hydroxylase gene of phenylketonuria in St Petersburg

Published:1996-09 Issue:5 Volume:19 Page:705-705
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Baranovskaya S.,Shevtsov S.,Maksimova S.,Kuzmin A.,Schwartz E.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://www.springerlink.com/index/pdf/10.1007/BF01799853

Reference2 articles.

1. Eisensmith RC, Okano Y, Dasovich M, et al (1992) Multiple origin for phenylketonuria in Europe.Am J Hum Genet 51: 1355–1365.

2. Goltsov AA, Eisensmith RC, Konecki DS, et al (1992) Association between mutations and a VNTR in the human phenylalanine hydroxylase gene.Am J Hum Genet 51: 627–636.

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