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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
File Details
- File Properties
-
Mime type: application/pdf
File size: 3502.1 kB