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Comprehensive analysis on phenotype and genetic basis of Chinese Fanconi anemia patients: dismal outcomes call for nationwide studies

2020-06-29

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Fanconi anemia (FA) is the most common inherited bone marrow failure (BMF) syndrome with 22 related genes identified. The <italic>ALDH2</italic> rs671variant has been proved related to accelerate the progression of BMF in FA patients. The phenotype and genetic basis of Chinese FA patients have not been investigated yet.<bold>Methods: </bold>We analyzed the 22 FA...

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Literature Corpus work
d6e358d8-839d-5a53-8a1a-703f7fb4ec01
DOI
10.21203/rs.2.16038/v6
Open publication

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Comprehensive analysis on phenotype and genetic basis of Chinese Fanconi anemia patients: dismal outcomes call for nationwide studiesDOI 10.21203/rs.2.16038/v6
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