Histochemical Abnormalities in Various Forms of Congenital Muscular Dystrophy

Authors

  • J Gordon Millichap Northwestern University Feinberg School of Medicine

DOI:

https://doi.org/10.15844/pedneurbriefs-22-3-2

Keywords:

Congenital Muscular Dystrophy, Glycosylated-A-Dystroglycan, Molecular Diagnostic Testing

Abstract

A large Australasian cohort of patients with congenital muscular dystrophy (CMD) was screened to determine the frequency of various forms, in a study at Children's Hospital at Westmead; the University of Sydney; University of Melbourne, Australia; and University of Nevada, Reno; and University of Illinois, Chicago.

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Published

2008-03-01

Issue

Vol 22, No 03 | Mar 2008

Section

Neuromuscular Disorders

License

Copyright (c) 2008 The Author(s)

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