Nemaline Myopathy Caused by Mutations in the Muscle α-Skeletal-Actin Gene-Reference-Cited by-同舟云学术

Nemaline Myopathy Caused by Mutations in the Muscle α-Skeletal-Actin Gene

Published:2001-06 Issue:6 Volume:68 Page:1333-1343
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ilkovski Biljana,Cooper Sandra T.,Nowak Kristen,Ryan Monique M.,Yang Nan,Schnell Christina,Durling Hayley J.,Roddick Laurence G.,Wilkinson Ian,Kornberg Andrew J.,Collins Kevin J.,Wallace Geoff,Gunning Peter,Hardeman Edna C.,Laing Nigel G.,North Kathryn N.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference30 articles.

1. Regulation and kinetics of the actin-myosin-ATP interaction;Adelstein;Annu Rev Biochem,1980

2. The structure and function of α-actinin;Blanchard;J Muscle Res Cell Motil,1989

3. Skeletal actin mRNA increases in the human heart during ontogenic development and is the major isoform of control and failing adult hearts;Boheler;J Clin Invest,1991

4. Reappearance of the minor α-sarcomeric actins in postnatal muscle;Collins;Am J Physiol,1997

5. Mutations in the β-tropomyosin (TPM2) gene in rare cases of autosomal dominant nemaline myopathy. World Muscle Society abstract;Donner;Neuromuscul Disord,2000

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