✦ LIBER ✦
Detection of 53 FBN1 mutations (41 novel and 12 recurrent) and genotype–phenotype correlations in 113 unrelated probands referred with Marfan syndrome, or a related fibrillinopathy
✍ Scribed by C.L.S. Turner; H. Emery; A.L. Collins; R.J. Howarth; C.M. Yearwood; E. Cross; P.J. Duncan; D.J. Bunyan; J.F. Harvey; N.C. Foulds
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 223 KB
- Volume
- 149A
- Category
- Article
- ISSN
- 1552-4825
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