The identification of several new genes responsible for different forms of congenital muscular dystrophies (CMD) has dramatically expanded our knowledge on the spectrum of these conditions and their pathogenesis, allowing a better characterization of the individual forms and of the specific pathomechanisms underlying them.
CITATION STYLE
Mercuri, E., & Muntoni, F. (2015). Congenital Muscular Dystrophies. In Neuromuscular Disorders of Infancy, Childhood, and Adolescence: A Clinician’s Approach (pp. 538–550). Elsevier Inc. https://doi.org/10.1016/B978-0-12-417044-5.00029-9
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