Open AccessFrequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population is c.-160 A>G
Author(s) -
Burhan Balta,
Murat Erdoğan,
Aslıhan Kiraz,
Serdal Korkmaz,
Alperen Ağadayı
Publication year - 2018
Publication title -
turkish journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.351
H-Index - 16
ISSN - 1300-7777
DOI - 10.4274/tjh.2018.0194
Subject(s) - medicine , turkish population , turkish , genetics , mutation , gene , population , genotype , biology , environmental health , linguistics , philosophy
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