ISSN:
1546-1718
Source:
Nature Archives 1869 - 2009
Topics:
Biology
,
Medicine
Notes:
[Auszug] Sir — Like mutations in most heritable disorders of connective tissue, fibrillin-1 (FBN1) mutations in the spectrum of the Marfan syndrome (MFS) are most often private (see ref. 1 for review). Thus, finding an identical molecular change in more than one affected individual or family has been ...
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1038/ng0197-12
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