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Pediatric Neurology Briefs: Volume 06, Issue 10

Werdnig-Hoffmann: Dominant Inheritance Open Access (recommended)

Descriptions

Resource type(s)
Article
Keyword
Autosomal Dominant Inheritance
Werdnig-Hoffmann Disease
Neonatal Adrenoleukodystrophy
Rights
Attribution 4.0 International

Creator
Millichap, J. Gordon
Abstract
A family in which both Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy occurred, with apparent autosomal dominant inheritance, is reported from the Department of Neurology, Mayo Clinic Jacksonville, FL and Johns Hopkins University School of Medicine, Baltimore, MD.
Publisher
DigitalHub. Galter Health Sciences Library
Pediatric Neurology Briefs Publishers
Date Created
1992
Original Identifier
PNB-6-78-b
Language
English
Subject: MESH
Neurosurgery
Child
Brain Diseases
Pediatrics
Neurology
Nervous System Diseases
Child Development
Infant
DOI
10.15844/pedneurbriefs-6-10-7

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