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Article

Congenital myasthenia syndrome with demyelinating sensorimotor neuropathy responsive to salbutamol monotherapy: a novel clinical phenotype of CHRNE mutation.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Jul 2024

Ghosh Ritwik, Dubey Souvik, Roy Dipayan, Mayo Sonia, Benito-León Julián

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Share to Adrenergic beta-2 Receptor Agonists
Share to Albuterol
Share to Demyelinating Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Myasthenic Syndromes, Congenital

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Share to Receptors, Cholinergic

Source

Identifiers

PMID: 38411853
DOI: 10.1007/s10072-024-07420-z

Genes

CHRNE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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