Messenger RNA processing is altered in autosomal dominant leukodystrophy-Reference-Cited by-同舟云学术

Messenger RNA processing is altered in autosomal dominant leukodystrophy

Published:2015-01-30 Issue:10 Volume:24 Page:2746-2756
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Bartoletti-Stella A.,Gasparini L.,Giacomini C.,Corrado P.,Terlizzi R.,Giorgio E.,Magini P.,Seri M.,Baruzzi A.,Parchi P.,Brusco A.,Cortelli P.,Capellari S.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/24/10/2746/14143116/ddv034.pdf

Reference65 articles.

1. Nuclear lamins: Functions and clinical implications

2. Lamin B1 duplications cause autosomal dominant leukodystrophy

3. Analysis of LMNB 1 Duplications in Autosomal Dominant Leukodystrophy Provides Insights into Duplication Mechanisms and Allele‐Specific Expression

4. A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations

5. Insertional Mutation of the Drosophila Nuclear Lamin Dm0 Gene Results in Defective Nuclear Envelopes, Clustering of Nuclear Pore Complexes, and Accumulation of Annulate Lamellae

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