Burhan BALTA, Murat ERDOĞAN, Aslıhan KİRAZ, Serdal KORKMAZ, Alperen AĞADAYI

A Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G

Türk Toplumunda Hiperferritinemi Katarakt Sendromuna Neden Olan FTL Genindeki Yaygın Mutasyon c.-160A>G’dir

Turkish Journal of Hematology

2019-Cilt: 36 - Sayı: 1

25-28

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