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Literature DB >> 7807958

Cognitive development related to metabolic phenotype and mutation genotype in 25 Hungarian patients with phenylketonuria.

A Schuler¹, C Somogyi, M Máté, L Pataki, I Törös, S L Woo, R C Eisensmith, G Fekete.

Abstract

Entities: Disease Species

Mesh：

Year: 1994 PMID： 7807958 DOI： 10.1007/bf00711835

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

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1 in total

1. Molecular basis of phenotypic heterogeneity in phenylketonuria.

Authors: Y Okano; R C Eisensmith; F Güttler; U Lichter-Konecki; D S Konecki; F K Trefz; M Dasovich; T Wang; K Henriksen; H Lou
Journal: N Engl J Med Date: 1991-05-02 Impact factor: 91.245

1 in total

1. A longitudinal study of phenylketonuria based on the data of the Budapest Screening Center.

Authors: A Schuler; C Somogyi; I Tôrös; L Pataki; M Mété; E Kiss; A Nagy
Journal: Eur J Pediatr Date: 1996-07 Impact factor: 3.183

1 in total