Back to Search
Start Over
Recurrent and founder mutations in the Netherlands: Extensive clinical variability in Marfan syndrome patients with a single novel recurrent fibrillin-1 missense mutation*.
- Source :
- Founder Mutations in Inherited Cardiac Diseases in the Netherlands; 2014, p89-94, 6p
- Publication Year :
- 2014
Details
- Language :
- English
- ISBNs :
- 9789036807043
- Database :
- Complementary Index
- Journal :
- Founder Mutations in Inherited Cardiac Diseases in the Netherlands
- Publication Type :
- Book
- Accession number :
- 98755378
- Full Text :
- https://doi.org/10.1007/978-90-368-0705-0_12