FANCA and contribution of studies from Asian populations to the understanding of fanca mediated Fanconi anemia
Fanconi anemia (FA) is a recessive disorder known to cause hematological and several congenital deformities in affected individuals worldwide. Out of 22 known FA causative genes, mutations in Fanconi Anemia Complementation Group A (FANCA) accounts for 60%-70% of FA cases. FANCA is a multi-f...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
Serbian Genetics Society
2019-01-01
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Series: | Genetika |
Subjects: | |
Online Access: | http://www.doiserbia.nb.rs/img/doi/0534-0012/2019/0534-00121903197S.pdf |