Hyperphenylalaninemia in the Czech Republic: genotype-phenotype correlations and in silico analysis of novel missense mutations.

Réblová, Kamila

Hyperphenylalaninemia in the Czech Republic: genotype-phenotype correlations and in silico analysis of novel missense mutations. [electronic resource] - Clinica chimica acta; international journal of clinical chemistry Apr 2013 - 1-10 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1873-3492

10.1016/j.cca.2013.01.006 doi


Computational Biology
Computer Simulation
Czech Republic
Genetic Association Studies
Genotype
Humans
Molecular Dynamics Simulation
Mutation, Missense--genetics
Phenotype
Phenylketonurias--diagnosis