Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review

بواسطة Tanu Tangsricharoen, Rungrote Natesirinilkul, Arunee Phusua, Kanda Fanhchaksai, Chupong Ittiwut, Wanna Chetruengchai, Monthana Juntharaniyom, Pimlak Charoenkwan, Vip Viprakasit, Chureerat Phokaew, Vorasuk Shotelersuk
منشور في 2022

Mutations in Krüppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression

بواسطة Vip Viprakasit, Supachai Ekwattanakit, Suchada Riolueang, Nipon Chalaow, Chris Fisher, Karen Lower, Hitoshi Kanno, Kalaya Tachavanich, Sasithorn Bejrachandra, Jariya Saipin, Monthana Juntharaniyom, Kleebsabai Sanpakit, Voravarn S. Tanphaichitr, Duantida Songdej, Christian Babbs, Richard J. Gibbons, Sjaak Philipsen, Douglas R. Higgs
منشور في 2018