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Article

Diagnosis of congenital myasthenic syndrome with mutation of the RAPSN gene after general anaesthesia.

European journal of anaesthesiology - 1 Oct 2011

Gentili Andrea, Ansaloni Stefania, Morello William, Cecini Maria T, Cordelli Duccio M, Baroncini Simonetta

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21372719
DOI: 10.1097/EJA.0b013e3283453f4b

Genes

RAPSN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Diagnosis of congenital myasthenic syndrome with mutation of the RAPSN gene after general anaesthesia.PMID 21372719Read ↗

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Unique presentation of rapidly fluctuating symptoms in a child with congenital myasthenic syndrome due to RAPSN mutation.Semantic proximity Read ↗

Late diagnosis of RAPSN mutation-associated congenital myasthenic syndrome with obstructive sleep apnea in a 5-year-old girl.Semantic proximity Read ↗

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A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndrome.Semantic proximity Read ↗

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