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Ectopia lentis, chorioretinal dystrophy and myopia

✍ Scribed by Kenneth G. Noble; Sherry Bass; Jerome Sherman


Book ID
105117621
Publisher
Springer-Verlag
Year
1993
Tongue
English
Weight
573 KB
Volume
83
Category
Article
ISSN
0012-4486

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## Abstract Mutations of the fibrillin‐1 (__FBN1__) gene on chromosome 15 have been described in patients with classical Marfan syndrome (MFS), neonatal MFS, the β€œMASS” phenotype, autosomal dominant ascending aortic aneurysms, autosomal dominant ectopia lentis (EL), Marfanoid skeletal features [Mil