Congenital myasthenic syndrome due to heteroallelic nonsense/missense mutations 
in the acetylcholine receptor epsilon subunit gene

Kraner, S; Burgunder, JM; Rosler, KM; Steinlein, OK; Sieb, JP

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Congenital myasthenic syndrome due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene

Kraner, S., Burgunder, J., Rosler, K., Steinlein, O., & Sieb, J. (2002). Congenital myasthenic syndrome due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene. European Journal of Neurology, 9(6), 694-695.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-000E-A017-3 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-000E-A018-1

Genre: Journal Article

Alternative Title : Eur. J. Neurol.

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Creators:
Kraner, S¹, Author
Burgunder, JM¹, Author
Rosler, KM¹, Author
Steinlein, OK¹, Author
Sieb, JP¹, Author

Affiliations:
1Max Planck Institute of Psychiatry, Max Planck Society, ou_1607137

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Free keywords: acetylcholine receptor; channelopathies; end-plate; fatigue; muscular weakness

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Language(s): eng - English

Dates: Date issued: 2002-11

Publication Status: Issued

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Rev. Type: Peer

Identifiers: eDoc: 4037
ISI: 000179547400026

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Title: European Journal of Neurology

Alternative Title : Eur. J. Neurol.

Source Genre: Journal

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Pages: - Volume / Issue: 9 (6) Sequence Number: - Start / End Page: 694 - 695 Identifier: ISSN: 1351-5101