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Research ArticleArticle

Substitutions of the Highly Conserved M2 Leucine Create Spontaneously Opening ρ1 γ-Aminobutyric Acid Receptors

Yongchang Chang and David S. Weiss
Molecular Pharmacology March 1998, 53 (3) 511-523; DOI: https://doi.org/10.1124/mol.53.3.511
Yongchang Chang
Departments of Neurobiology and Physiology & Biophysics, University of Alabama at Birmingham, Birmingham, Alabama 35294
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David S. Weiss
Departments of Neurobiology and Physiology & Biophysics, University of Alabama at Birmingham, Birmingham, Alabama 35294
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Article Information

vol. 53 no. 3 511-523
DOI 
https://doi.org/10.1124/mol.53.3.511
PubMed 
9495819

Published By 
American Society for Pharmacology and Experimental Therapeutics
Print ISSN 
0026-895X
Online ISSN 
1521-0111
History 
  • Received July 15, 1997
  • Accepted November 12, 1997
  • Published online March 1, 1998.

Copyright & Usage 
The American Society for Pharmacology and Experimental Therapeutics

Author Information

  1. Yongchang Chang and
  2. David S. Weiss
  1. Departments of Neurobiology and Physiology & Biophysics, University of Alabama at Birmingham, Birmingham, Alabama 35294
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Molecular Pharmacology: 53 (3)
Molecular Pharmacology
Vol. 53, Issue 3
1 Mar 1998
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Research ArticleArticle

Substitutions of the Highly Conserved M2 Leucine Create Spontaneously Opening ρ1 γ-Aminobutyric Acid Receptors

Yongchang Chang and David S. Weiss
Molecular Pharmacology March 1, 1998, 53 (3) 511-523; DOI: https://doi.org/10.1124/mol.53.3.511

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Research ArticleArticle

Substitutions of the Highly Conserved M2 Leucine Create Spontaneously Opening ρ1 γ-Aminobutyric Acid Receptors

Yongchang Chang and David S. Weiss
Molecular Pharmacology March 1, 1998, 53 (3) 511-523; DOI: https://doi.org/10.1124/mol.53.3.511
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