Molecular Characterization of Glucose-6-phosphate Dehydrogenase Deficiency in Families from the Republic of Macedonia and Genotype-phenotype Correlation

INTRODUCTION: Glucose-6-phospahte dehydrogenase deficiency (G6PD) is one of the most common inherited disorders affecting around 400 million people worldwide. Molecular analysis of the G6PD gene identified more than 140 distinct mutations, the majority being single base missense mutations. G6PD Medi...

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Bibliografski detalji
Izdano u:Med Arch
Glavni autori: Cherepnalkovski, Anet Papazovska, Zemunik, Tatijana, Glamocanin, Sofijanka, Piperkova, Katica, Gunjaca, Ivana, Kocheva, Svetlana, Jovanova, Biljana Coneska, Krzelj, Vjekoslav
Format: Artigo
Jezik:Inglês
Izdano: AVICENA, d.o.o., Sarajevo 2015
Teme:
Original Paper
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4639331/
https://ncbi.nlm.nih.gov/pubmed/26622077
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5455/medarh.2015.69.284-288
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