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

BACKGROUND: Fanconi anemia (FA) is the most common inherited bone marrow failure (BMF) syndrome with 22 related genes identified. The ALDH2 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 i...

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Detalles Bibliográficos
Autores principales: Nie, Daijing, Zhang, Jing, Wang, Fang, Zhang, Wei, Liu, Lili, Chen, Xue, Zhang, Yang, Cao, Panxiang, Xiong, Min, Wang, Tong, Wu, Ping, Ma, Xiaoli, Tian, Wenjun, Wang, Mangju, Chen, Kylan N., Liu, Hongxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268325/
https://www.ncbi.nlm.nih.gov/pubmed/32487094
http://dx.doi.org/10.1186/s12881-020-01057-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268325/
https://www.ncbi.nlm.nih.gov/pubmed/32487094
http://dx.doi.org/10.1186/s12881-020-01057-3

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