Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutations
Author:
Publisher
Oxford University Press (OUP)
Subject
Neurology (clinical)
Link
http://academic.oup.com/brain/article-pdf/133/5/1451/16697370/awq083.pdf
Reference22 articles.
1. Growth and muscle defects in mice lacking adult myosin heavy chain genes;Acakpo-Satchivi;J Cell Biol,1997
2. Postnatal myosin heavy chain isoform expression in normal mice and mice null for IIb or IId myosin heavy chains;Allen;Dev Biol,2001
3. Inactivation of myosin heavy chain genes in the mouse: diverse and unexpected phenotypes;Allen;Microsc Res Tech,2000
4. Mutation of the IIB myosin heavy chain gene results in muscle fiber loss and compensatory hypertrophy;Allen;Am J Physiol Cell Physiol,2001
5. Myosin heavy and light chain expression during human skeletal muscle development and precocious muscle maturation induced by thyroid hormone;Butler-Browne;Anat Embryol (Berl),1990
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