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Pediatric Neurology Briefs: Volume 15, Issue 10

Nemaline Myopathy: Clinical Study Open Access (recommended)

Descriptions

Resource type(s)
Article
Keyword
Neonatal Hypotonia
Arthrogryposis Multiplex Congenita
Nemaline Myopathy
Rights
Attribution 4.0 International

Creator
Millichap, J. Gordon
Abstract
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; Childrens Hospital, Boston; and other centers.
Publisher
DigitalHub. Galter Health Sciences Library
Pediatric Neurology Briefs Publishers
Date Created
2001
Original Identifier
PNB-15-73
Language
English
Subject: MESH
Neurology
Child
Infant
Pediatrics
Nervous System Diseases
Child Development
Brain Diseases
Neurosurgery
DOI
10.15844/pedneurbriefs-15-10-1

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