Literature DB >> 8892033

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

S Baranovskaya1, S Shevtsov, S Maksimova, A Kuzmin, E Schwartz.   

Abstract

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Year:  1996        PMID： 8892033     DOI： 10.1007/bf01799853

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  2 in total

1.  Associations between mutations and a VNTR in the human phenylalanine hydroxylase gene.

Authors:  A A Goltsov; R C Eisensmith; D S Konecki; U Lichter-Konecki; S L Woo
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

2.  Multiple origins for phenylketonuria in Europe.

Authors:  R C Eisensmith; Y Okano; M Dasovich; T Wang; F Güttler; H Lou; P Guldberg; U Lichter-Konecki; D S Konecki; E Svensson
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025
  2 in total
  2 in total

1.  Hyperphenylalaninaemias in Estonia: Genotype-Phenotype Correlation and Comparative Overview of the Patient Cohort Before and After Nation-Wide Neonatal Screening.

Authors:  Hardo Lilleväli; Karit Reinson; Kai Muru; Kristi Simenson; Ülle Murumets; Tõnu Möls; Katrin Õunap
Journal:  JIMD Rep       Date:  2017-09-28

2.  Association Between PAH Mutations and VNTR Alleles in the West Azerbaijani PKU Patients.

Authors:  Morteza Bagheri; Isa Abdi Rad; Nima Hosseini Jazani; Rasoul Zarrin; Ahad Ghazavi
Journal:  Maedica (Buchar)       Date:  2014-09
  2 in total

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