English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  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.

Item is

Files

show Files

Locators

show

Creators

show
hide
 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              

Content

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

Details

show
hide
Language(s): eng - English
 Dates: 2006
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 305368
ISI: 000240275000011
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Biochemical and Biophysical Research Communications
  Alternative Title : Biochem. Biophys. Res. Commun.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 348 (2) Sequence Number: - Start / End Page: 400 - 405 Identifier: ISSN: 0006-291X