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Human molecular genetics and the elucidation of the primary biochemical defect in duchenne muscular dystrophy

✍ Scribed by Hoffman, Eric P.

Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
534 KB
Volume
14
Category
Article
ISSN
0886-1544

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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