A R644C mutation within lamin A extends the mutations causing dilated cardiomyopathy.

Human mutation ·Vol. 17 ·No. 2 ·2001-02-00 ·Pages 154

Genschel J, Bochow B, Kuepferling S, Ewert R, Hetzer R, Lochs H, Schmidt H

Abstract

暂无摘要

MeSH Terms

Amino Acid Substitution Cardiomyopathy, Dilated/genetics,pathology DNA/chemistry,genetics DNA Mutational Analysis Humans Lamin Type A Lamins Mutation, Missense Nuclear Proteins/genetics

Chemicals

Lamin Type A Lamins Nuclear Proteins DNA

Authors & Affiliations

7 authors, click to expand affiliations / ORCID

Genschel J

Campus Charite Mitte, Med. Klinik m.S. Gastroenterologie, Hepatologie und Endokrinologie, Berlin.

Bochow B

Kuepferling S

Ewert R

Hetzer R

Lochs H

Schmidt H

Article Info

Journal

Human mutation

Abbr.

Hum Mutat

ISSN

1098-1004

DOI

10.1002/1098-1004(200102)17:2<154::AID-HUMU11>3.0.CO;2-R

Published

2001-02-00

Pages

154

Language

English

Region

United States

NLM ID

9215429

Subset

External Links

PubMed source DOI: 10.1002/1098-1004(200102)17:2<154::AID-HUMU11>3.0.CO;2-R View journal details

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A R644C mutation within lamin A extends the mutations causing dilated cardiomyopathy.

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