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Article

Congenital myasthenic syndrome due to a novel missense mutation in the gene encoding choline acetyltransferase

1 Mar 2003

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 12609506
DOI: 10.1016/s0960-8966(02)00273-0

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Source receipt: pubmed, retrieved 7 Sept 2026.

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Congenital myasthenic syndrome due to a novel missense mutation in the gene encoding choline acetyltransferasePMID 12609506Read ↗

Congenital Myasthenic Syndrome due to a Novel Mutation in CHAT Gene.Semantic proximity Read ↗

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