Novel delta subunit mutation in slow-channel syndrome causes severe weakness by novel mechanisms-Reference-Cited by-同舟云学术

Novel delta subunit mutation in slow-channel syndrome causes severe weakness by novel mechanisms

Published:2002-01 Issue:1 Volume:51 Page:102-112
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Gomez Christopher M.,Maselli Ricardo A.,Vohra Bhupinder P. S.,Navedo Manuel,Stiles Joel R.,Charnet Pierre,Schott Kelly,Rojas Legier,Keesey John,Verity Anthony,Wollmann Robert W.,Lasalde-Dominicci Jose

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference30 articles.

1. A newly recognized congenital myasthenic syndrome attributed to a prolonged open time of the acetylcholine-induced ion channel

2. Myasthenic syndromes. In: eds. Myology. 2nd ed. New York: McGraw-Hill, 1994; 393-418.

3. A ?-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndrome

4. Slow-Channel Myasthenic Syndrome Caused By Enhanced Activation, Desensitization, and Agonist Binding Affinity Attributable to Mutation in the M2 Domain of the Acetylcholine Receptor α Subunit

5. A leucine‐to‐phenylalanine substitution in the acetylcholine receptor ion channel in a family with the slow‐channel syndrome

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