Apert syndrome (AS) is a severe disorder, characterized by craniosynostosis and complex syndactyly of the hands and feet. Two heterozygous gain-of-function substitutions (Ser252Trp and Pro253Arg) in exon IIIa of fibroblast growth factor receptor 2 (FGFR2) are responsible for 498% of cases. Here we d
✦ LIBER ✦
An insertion/deletion in the porcine FGFR2 gene
✍ Scribed by J. Aldenhoven; A. Spötter; O. Distl
- Book ID
- 108899961
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 484 KB
- Volume
- 124
- Category
- Article
- ISSN
- 0931-2668
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