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Article

Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations.

Journal of neuropathology and experimental neurology - 1 Nov 2008

Vallat Jean-Michel, Ouvrier Robert A, Pollard John D, Magdelaine Corinne, Zhu Danqing, Nicholson Garth A, Grew Simon, Ryan Monique M, Funalot Benoît

Abstract excerpt

Neuropathologic abnormalities can be sufficiently characteristic to suggest the genetic basis of some hereditary neuropathies such as those associated with mutations in MPZ, GJB1, GDAP1, MTMR2, SH3TC2, PRX, FGD4, and LMNA. We analyzed the morphologic features of 9 sural nerve biopsies from 6 pati...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18957892
DOI: 10.1097/NEN.0b013e31818b6cbc

Genes

FGD4
GDAP1
GJB1
LMNA
MPZ
MTMR2
PRX

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18957892-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations.PMID 18957892Read ↗

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