Systematic evaluation of paediatric cohort with iron refractory iron deficiency anaemia (IRIDA) phenotype reveals multiple TMPRSS6 gene variations.
第一作者:
Prateek,Bhatia
第一单位:
Paediatric Haematology-Oncology Unit, Department of Paediatrics, Advanced Paediatric Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
作者:
医学主题词
贫血, 缺铁性(Anemia, Iron-Deficiency);病例对照研究(Case-Control Studies);儿童, 学龄前(Child, Preschool);队列研究(Cohort Studies);女(雌)性(Female);遗传变异(Genetic Variation);人类(Humans);男(雄)性(Male);膜蛋白质类(Membrane Proteins);突变(Mutation);表型(Phenotype);丝氨酸内肽酶类(Serine Endopeptidases)
DOI
10.1111/bjh.14554
PMID
28169443
发布时间
2018-02-08
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