Nemaline Myopathy: Clinical Study
DOI:
https://doi.org/10.15844/pedneurbriefs-15-10-1Keywords:
Nernaline Myopathy, Arthrogryposis Multiplex Congenita, Neonatal HypotoniaAbstract
Clinical and genetic characteristics, prognostic risk factors, and classification of nemaline myopathy (NM) are examined in a study of 143 cases identified at two centers in Australia and North America and reported from the Neurogenetics Research Unit, University of Sydney, Australia; Children’s Hospital, Boston; and other centers.Published
2001-10-01
Issue
Section
Neuromuscular Disorders
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Copyright (c) 2001 The Author(s)
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