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Myopathy, Centronuclear, Autosomal Dominant

Known as: MYOTUBULAR MYOPATHY, AUTOSOMAL DOMINANT, MYOPATHY, CENTRONUCLEAR, 1, Centronuclear Myopathy 1 
A myopathy inherited in an autosomal dominant or recessive pattern, caused by mutations in the DNM2, BIN1, and TTN genes. Microscopically there is… 
National Institutes of Health

Related topics

Related topics

9 relations
Autosomal dominant inheritanceBlepharoptosisCongenital Structural MyopathyConnective and Soft Tissue

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Bio-economic and operational feasibility of introducing oestrus synchronization and artificial insemination in simulated smallholder sheep breeding programmes.
Low selection intensity due to few selection candidates available at any one time due to thinly spread year-round lambings in… 
2016
2016
DNM2 mutations in Chinese Han patients with centronuclear myopathy
Centronuclear myopathy (CNM) is a congenital myopathy characterized by an abnormally high number of muscle fibers with centrally… 
2012
2012
A STUDY OF RISK FACTORS AMONG HIGH SCHOOL STUDENTS IN THE COMMONWEALTH OF THE NORTHERN MARIANA ISLANDS Research and Development Cadre
The status of students at risk of failure in public high schools in the Commonwealth of the Northern Mariana Islands (CNMI) was… 
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