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Article

Mutations of the same sequence of the myelin P0 gene causing two different phenotypes.

Human mutation - 1 Jan 1998

Schiavon F, Rampazzo A, Merlini L, Angelini C, Mostacciuolo M L

Abstract excerpt

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Share to Amino Acid Substitution
Share to Charcot-Marie-Tooth Disease
Share to DNA
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Myelin P0 Protein

Share to Point Mutation

Share to Polymorphism, Single-Stranded Conformational

Share to Sequence Deletion

Source

Identifiers

PMID: 9452091
DOI: 10.1002/humu.1380110170

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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