✦ LIBER ✦
An FBN1 Deep Intronic Mutation in a Familial Case of Marfan Syndrome: An Explanation for Genetically Unsolved Cases?
✍ Scribed by Gillis, Elisabeth; Kempers, Marlies; Salemink, Simone; Timmermans, Janneke; Cheriex, Emile C.; Bekkers, Sebastiaan C.A.M.; Fransen, Erik; De Die-Smulders, Christine E.M.; Loeys, Bart L.; Laer, Lut Van
- Book ID
- 123621574
- Publisher
- John Wiley and Sons
- Year
- 2014
- Tongue
- English
- Weight
- 550 KB
- Volume
- 35
- Category
- Article
- ISSN
- 1059-7794
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