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  Mutations within the human GLYT2 (SLC6A5) gene associated with hyperekplexia

Eulenburg, V., Becker, K., Gomeza, J., Schmitt, B., Becker, C. M., & Betz, H. (2006). Mutations within the human GLYT2 (SLC6A5) gene associated with hyperekplexia. Biochemical and Biophysical Research Communications, 348(2), 400-405.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-002E-1EB2-2 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-002E-1EB3-F
Genre: Journal Article

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 Creators:
Eulenburg, V.1, Author           
Becker, K., Author
Gomeza, J.1, Author           
Schmitt, B.1, Author           
Becker, C. M., Author
Betz, H.1, Author           
Affiliations:
1Neurochemistry Department, Max Planck Institute for Brain Research, Max Planck Society, ou_2461704              

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Free keywords: glycine transporter 2; hyperekplexia; disease mutation
 Abstract: -

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Language(s): eng - English
 Dates: 2006
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 305368
ISI: 000240275000011
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Title: Biochemical and Biophysical Research Communications
  Alternative Title : Biochem. Biophys. Res. Commun.
Source Genre: Journal
 Creator(s):
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Publ. Info: -
Pages: - Volume / Issue: 348 (2) Sequence Number: - Start / End Page: 400 - 405 Identifier: ISSN: 0006-291X