Evidence for neuroaxonal injury in patients with proteolipid gene mutations

Letter/Communication

J Garbern, M Shy, K Krajewski, J Kamholz, G Hobson and F Cambi

Neurology, Vol.57(10), pp.1938-1939

11/27/2001

DOI: 10.1212/WNL.57.10.1938-a

PMID: 11723304

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Neuroaxonal Dystrophies - diagnosis

Magnetic Resonance Spectroscopy

DNA Mutational Analysis

Myelin Proteolipid Protein - genetics

Axons - pathology

Humans

Brain - pathology

Female

Male

Mutation - genetics

Neuroaxonal Dystrophies - genetics

Genetic Carrier Screening

Title: Subtitle: Evidence for neuroaxonal injury in patients with proteolipid gene mutations
Creators: J Garbern
M Shy
K Krajewski
J Kamholz
G Hobson
F Cambi
Resource Type: Letter/Communication
Publication Details: Neurology, Vol.57(10), pp.1938-1939
Publisher: United States
DOI: 10.1212/WNL.57.10.1938-a
PMID: 11723304
ISSN: 0028-3878
eISSN: 1526-632X
Language: English
Date published: 11/27/2001
Academic Unit: Neurology; Molecular Physiology and Biophysics; Psychiatry; Stead Family Department of Pediatrics; Iowa Neuroscience Institute
Record Identifier: 9984020624002771

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