Recurrent and founder mutations in the Netherlands. Extensive clinical variability in Marfan syndrome patients with a single novel recurrent fibrillin-1 missense mutations.
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Publication year
2010Source
Netherlands Heart Journal, 18, 2, (2010), pp. 85-9ISSN
Publication type
Article / Letter to editor
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Organization
Human Genetics
Biochemistry (UMC)
Journal title
Netherlands Heart Journal
Volume
vol. 18
Issue
iss. 2
Page start
p. 85
Page end
p. 9
Subject
DCN 2: Functional Neurogenomics; IGMD 3: Genomic disorders and inherited multi-system disordersThis item appears in the following Collection(s)
- Academic publications [238426]
- Electronic publications [122508]
- Faculty of Medical Sciences [90358]
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