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Hereditary muscular dystrophy in mdx mice as a homologous model for introduction of cell technologies in the treatment of progressive muscular dystrophies in humans

✍ Scribed by M. A. Stenina; V. I. Savchuk; V. F. Sitnikov; L. I. Krivov; A. B. Kuznetsov; D. A. Voevodin; V. N. Yarygin; G. T. Sukhikh

Publisher: Springer US
Year: 2004
Tongue: English
Weight: 340 KB
Volume: 138
Category: Article
ISSN: 0007-4888
DOI: 10.1007/s10517-005-0118-4

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## Abstract Duchenne muscular dystrophy is an X‐linked recessive genetic disease characterized by severe skeletal muscular degeneration. The placenta is considered to be a promising candidate cell source for cellular therapeutics because it contains a large number of cells and heterogenous cell pop