Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/58336
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dc.contributor.authorSaranyapin Potikanonden_US
dc.contributor.authorWutigri Nimlamoolen_US
dc.contributor.authorJasprien Noordermeeren_US
dc.contributor.authorLee G. Fradkinen_US
dc.date.accessioned2018-09-05T04:22:50Z-
dc.date.available2018-09-05T04:22:50Z-
dc.date.issued2018-01-01en_US
dc.identifier.issn22148019en_US
dc.identifier.issn00652598en_US
dc.identifier.other2-s2.0-85049368882en_US
dc.identifier.other10.1007/978-981-13-0529-0_9en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85049368882&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/58336-
dc.description.abstract© 2018, Springer Nature Singapore Pte Ltd. Muscular dystrophy (MD) is a group of muscle weakness disease involving in inherited genetic conditions. MD is caused by mutations or alteration in the genes responsible for the structure and functioning of muscles. There are many different types of MD which have a wide range from mild symptoms to severe disability. Some types involve the muscles used for breathing which eventually affect life expectancy. This chapter provides an overview of the MD types, its gene mutations, and the Drosophila MD models. Specifically, the Duchenne muscular dystrophy (DMD), the most common form of MD, will be thoroughly discussed including Dystrophin genes, their isoforms, possible mechanisms, and signaling pathways of pathogenesis.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleMuscular dystrophy modelen_US
dc.typeBook Seriesen_US
article.title.sourcetitleAdvances in Experimental Medicine and Biologyen_US
article.volume1076en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsLeiden University Medical Center - LUMCen_US
article.stream.affiliationsUniversity of Massachusetts Medical Schoolen_US
Appears in Collections:CMUL: Journal Articles

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