Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy-Reference-Cited by-同舟云学术

Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

Published:2000-04 Issue:4 Volume:66 Page:1407-1412
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Raffaele di Barletta Marina,Ricci Enzo,Galluzzi Giuliana,Tonali Pietro,Mora Marina,Morandi Lucia,Romorini Alessandro,Voit Thomas,Orstavik Karen Helene,Merlini Luciano,Trevisan Carlo,Biancalana Valerie,Housmanowa-Petrusewicz Irena,Bione Silvia,Ricotti Roberta,Schwartz Ketty,Bonne Giselle,Toniolo Daniela

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference33 articles.

1. Identification of a novel X-linked gene responsible for Emery Dreifuss muscular dystrophy;Bione;Nat Genet,1994

2. Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease;Bione;Hum Mol Genet,1995

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

4. Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement;Brodsky;Circulation,2000

5. Nuclear lamin A/C R482 mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy;Cao;Hum Mol Genet,2000

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