Collections
This file is in the following collections:
| Pediatric Neurology Briefs: Volume 15, Issue 10 |
X-Linked Charcot-Marie-Tooth Disease in 93 Patients Open Access (recommended)
Descriptions
- Resource type(s)
- Article
- Keyword
- Molecular Genetic Testing
Nonfunctional Mutations
Electrophysiological and Genetic Features
- Rights
- Attribution 4.0 International
- Creator
-
Millichap, J. Gordon
- Abstract
-
The clinical, electrophysiological and genetic features of 93 patients (41 males, 52 females) from 37 unrelated families with X-linked dominant Charcot-Marie-Tooth (CMTX) disease are reported from the Hopital de la Salpetriere, Paris, France.
- Publisher
-
DigitalHub. Galter Health Sciences Library
Pediatric Neurology Briefs Publishers
- Date Created
-
2001
- Original Identifier
- PNB-15-76
- Language
- English
- Subject: MESH
-
Infant
Nervous System Diseases
Neurology
Brain Diseases
Neurosurgery
Child Development
Child
Pediatrics
- DOI
-
10.15844/pedneurbriefs-15-10-5
File Details
- File Properties
-
Mime type: application/pdf
File size: 2987.1 kB