Nemaline Myopathy: Clinical Study

Nemaline Myopathy: Clinical Study

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 Hos...

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Bibliographic Details
Main Author: J Gordon Millichap
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 2001-10-01
Series:Pediatric Neurology Briefs
Subjects:
nernaline myopathy
arthrogryposis multiplex congenita
neonatal hypotonia
Online Access:https://www.pediatricneurologybriefs.com/articles/1705
Description
Summary: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.
ISSN:1043-3155
2166-6482

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