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Article

[Non-fortuitous dynamin II mutation-related association: neutropenia and Charcot-Marie-Tooth disease].

Revue neurologique - 1 Apr 2012

Saint-Lézer A, Solé G, Ribeiro E, Latour P, Mercié P, Longy-Boursier M

Abstract excerpt

Charcot-Marie-Tooth (CMT) disease or hereditary motor and sensory neuropathy is a genetically and clinically heterogeneous group of disorders of the peripheral nervous system. Mutations in multiple genes are currently known. We report an original case of CMT associated with chronic neutropenia in a patient with a K562del mutation in the dynamin 2 (DNM2) gene in a patient presenting with alterated cognitive...

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Source

Identifiers

PMID: 22385972
DOI: 10.1016/j.neurol.2011.09.010

Genes

DNM2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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[Non-fortuitous dynamin II mutation-related association: neutropenia and Charcot-Marie-Tooth disease].PMID 22385972Read ↗

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