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Article

Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype.

Human molecular genetics - 1 Sept 1994

Rautenstrauss B, Nelis E, Grehl H, Pfeiffer R A, Van Broeckhoven C

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Share to DNA
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Share to Hereditary Sensory and Motor Neuropathy
Share to Myelin P0 Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 7530550
DOI: 10.1093/hmg/3.9.1701

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype.PMID 7530550Read ↗

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