Late onset Charcot-Marie-Tooth 2 syndrome caused by two novel mutations in the MPZ gene

Letter/Communication

John Kamholz and Michael E Shy

Neurology, Vol.63(1), pp.194; author reply 194-194

07/13/2004

DOI: 10.1212/WNL.63.1.194

PMID: 15249646

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Amino Acid Sequence

Humans

Myelin P0 Protein - genetics

Myelin P0 Protein - chemistry

Codon - genetics

Mutation, Missense

Amino Acid Substitution

Charcot-Marie-Tooth Disease - genetics

Title: Subtitle: Late onset Charcot-Marie-Tooth 2 syndrome caused by two novel mutations in the MPZ gene
Creators: John Kamholz
Michael E Shy
Resource Type: Letter/Communication
Publication Details: Neurology, Vol.63(1), pp.194; author reply 194-194
Publisher: United States
DOI: 10.1212/WNL.63.1.194
PMID: 15249646
ISSN: 0028-3878
eISSN: 1526-632X
Language: English
Date published: 07/13/2004
Academic Unit: Neurology; Molecular Physiology and Biophysics; Psychiatry; Stead Family Department of Pediatrics; Iowa Neuroscience Institute
Record Identifier: 9984020862902771

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