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A new model mouse for Duchenne muscular dystrophy produced by 2.4 Mb deletion of dystrophin gene using Cre-loxP recombination system
Authors:Kudoh Hiroe  Ikeda Haruko  Kakitani Makoto  Ueda Akiko  Hayasaka Michiko  Tomizuka Kazuma  Hanaoka Kazunori
Affiliation:Laboratory of Molecular Embryology, Department of Bioscience, Kitasato University School of Science, Sagamihara, Kanagawa 228-8555, Japan.
Abstract:
Keywords:mdx   DMD   Dystrophin   Cre-loxP   Muscle   Mouse   Dp427   Targeted mutagenesis   Chromosome engineering   Knock-out
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