Hyperphenylalaninemia in the Czech Republic: Genotype-phenotype correlations and in silico analysis of novel missense mutations;Corrigendum to “Hyperphenylalaninemia in the Czech Republic: genotype–phenotype correlations and in silico analysis of novel missense mutations” [Clin Chim Acta 419C: (2013) 1–10] (Clinica Chimica Acta (2013) 419 (1–10), (S0009898113000211), (10.1016/j.cca.2013.01.006))

Clinica Chimica Acta

Volumn 426, Issue , 2013, Pages 157-

  Réblová, Kamila ^a   Hrubá, Zuzana ^b   Procházková, Dagmar ^b   Pazdírková, Renata ^b   Pouchlá, Slávka ^b   Zeman, Jiří ^c,d   Fajkusová, Lenka ^a,b  

^a MASARYK UNIVERSITY   (Czech Republic)

^b UNIVERSITY HOSPITAL BRNO   (Czech Republic)

^c CHARLES UNIVERSITY   (Czech Republic)

^d CHARLES UNIVERSITY   (Czech Republic)

Author keywords

Hyperphenylalaninemia; Genotype phenotype relationship; Molecular modelling; Phenylalanine hydroxylase

Indexed keywords

ERRATUM;

EID: 85097332127     PISSN: 00098981     EISSN: 18733492     Source Type: Journal    
DOI: 10.1016/j.cca.2013.01.006     Document Type: Article

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