## How Fancbni anemia (FA) is a rare autosomal recessive disease characterized by diverse clinical symptoms, chromosomal instability, and hypersensitivity
Characterisation of two different nonsense mutations, C6792A and C6792G, causing skipping of exon 37 in the NF1 gene
β Scribed by L. Messiaen; Tom Callens; A. De Paepe; Margarita Craen; Geert Mortier
- Publisher
- Springer
- Year
- 1997
- Tongue
- English
- Weight
- 148 KB
- Volume
- 101
- Category
- Article
- ISSN
- 0340-6717
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