Fanconi anemia (FA) is a rare autosomal recessive disorder of hematopoiesis, with at least 11 complementation groups. FANCA, a gene for group A, accounts for the majority of FA patients. Previous studies of FANCA mutations revealed high allelic heterogeneity, frequent occurrence of large deletions,
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Identification of novel Asian Indian and Japanese mutations causing β-thalassaemia in the Egyptian population
✍ Scribed by N. El-Hashemite; Mary Petrou; A. S. Khalifa; N. M. Heshmat; Magdy S. Rady; Joy D. A. Delhanty
- Publisher
- Springer
- Year
- 1997
- Tongue
- English
- Weight
- 271 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0340-6717
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