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  Congenital myasthenic syndrome with episodic apnea in patients homozygous for a CHAT missense mutation

Kraner, S., Laufenberg, I., Strassburg, H. M., Sieb, J. P., & Steinlein, O. K. (2003). Congenital myasthenic syndrome with episodic apnea in patients homozygous for a CHAT missense mutation. Archives of Neurology, 60(5), 761-763.

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Genre: Journal Article
Alternative Title : Arch. Neurol.

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 Creators:
Kraner, S., Author
Laufenberg, I., Author
Strassburg, H. M., Author
Sieb, J. P.1, Author           
Steinlein, O. K., Author
Affiliations:
1Max Planck Institute of Psychiatry, Max Planck Society, ou_1607137              

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Language(s): eng - English
 Dates: 2003-05
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 121279
ISI: 000182867600015
 Degree: -

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Title: Archives of Neurology
  Alternative Title : Arch. Neurol.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 60 (5) Sequence Number: - Start / End Page: 761 - 763 Identifier: ISSN: 0003-9942