How Does a g993t Mutation in the Emerin Gene Cause Emery–Dreifuss Muscular Dystrophy?

Author： Holt I. Clements L. Manilal S. Morris G.E.

Publisher： Elsevier

ISSN： 0006-291X

Source： Biochemical and Biophysical Research Communications, Vol.287, Iss.5, 2001-10, pp. : 1129-1133

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Muscular dystrophy linked to a mutation in laminin

By Xu H. Wu X.-R. Wewer U.M. Engvall E.

Trends in Cell Biology, Vol. 5, Iss. 2, 1995-02 ,pp. : 59-59

Elsevier

Access to resources Recommend Favorite

Gene therapy for muscular dystrophy – a review ofpromising progress

By Gregorevic Paul Chamberlain Jeffrey S

Expert Opinion on Biological Therapy, Vol. 3, Iss. 5, 2003-08 ,pp. : 803-814

Informa Healthcare

Access to resources Recommend Favorite

AAV-directed muscular dystrophy gene therapy

By Tang Ying Cummins James Huard Johnny Wang Bing

Expert Opinion on Biological Therapy, Vol. 10, Iss. 3, 2010-03 ,pp. : 395-408

Informa Healthcare

Access to resources Recommend Favorite

Molecular dysfunction associated with the human mitochondrial 3302A>G mutation in the MTTL1 (mt-tRNA Leu(UUR) ) gene

By Maniura-Weber Katharina Helm Mark Engemann Katrin Eckertz Sabrina Möllers Myriam Schauen Matthias Hayrapetyan Armine von Kleist-Retzow Jürgen-Christoph Lightowlers Robert N. Bindoff Laurence A. Wiesner Rudolf J.

Nucleic Acids Research, Vol. 34, Iss. 22, 2006-12 ,pp. : 6404-6415

Oxford University Press

Access to resources Recommend Favorite

Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codon

By Rederstorff M.

Nucleic Acids Research, Vol. 36, Iss. 1, 2008-01 ,pp. : 237-244

Oxford University Press

Access to resources Recommend Favorite