Murat Erdoğan

4PUBLICATIONS
25CO-AUTHORS
NeurogeneticsPharmacogenomicsMedical infection agents (incl. prions)Cell and nuclear division
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Publications (4)

|Jun 15, 2026
Genotype-Phenotype Correlations in Phenylketonuria and Hyperphenylalaninemia: A Single-Center Study.

|Apr 17, 2025
A Rare Cause of Primary Microcephaly: 4 New Variants in CDK5RAP2 Gene and Review of the Literature.

Murat Erdogan, Aysel Unal, Muhammet Ensar Dogan

|Nov 08, 2018
Frequent Mutation in the <i>FTL</i> Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G

Burhan Balta, Murat Erdoğan, Aslıhan Kiraz

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