Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3′ terminus of the FBN1-gene-Reference-Cited by-同舟云学术

Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3′ terminus of the FBN1-gene

Published:2010-10-26 Issue:11 Volume:152A Page:2749-2755
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Graul-Neumann Luitgard M.,Kienitz Tina,Robinson Peter N.,Baasanjav Sevjidmaa,Karow Benjamin,Gillessen-Kaesbach Gabriele,Fahsold Raimund,Schmidt Hartmut,Hoffmann Katrin,Passarge Eberhard

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33690/fullpdf

Reference41 articles.

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