LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle-Reference-Cited by-同舟云学术

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LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle

Published:2011-12-20 Issue:7 Volume:21 Page:1544-1556
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Dialynas George,Flannery Kaitlin M.,Zirbel Luka N.,Nagy Peter L.,Mathews Katherine D.,Moore Steven A.,Wallrath Lori L.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference79 articles.

1. Human laminopathies: nuclei gone genetically awry;Nat. Rev. Genet.,2006

2. Hereditary muscular dystrophies and the heart;Neuromuscul. Disord.,2010

3. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery–Dreifuss muscular dystrophy;Nat. Genet.,1999

4. Novel LMNA mutations in patients with Emery–Dreifuss muscular dystrophy and functional characterization of four LMNA mutations;Hum. Mutat.,2011

5. The plant nuclear envelope;Cell. Mol. Life Sci.,2001

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