Linked Life Data

A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin.

Source:http://linkedlifedata.com/resource/pubmed/id/10534268

Neurology 1999 Oct 22 53 7 1564-9

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Authors

Rüdel R, Pongratz D, Janssen G, Brunner J, Mortier W, Lochmüller H, Seidel U, Karcagi V, Stucky J, Müller-Felber W, Jost W, Horváth R, Ramaekers V, Scharf P, Schlotter B, Herczegfalvi A, Abicht A

Affiliation

Genzentrum und Friedrich-Baur Institut, LMU München, Germany.

Abstract

Mutation analysis of the acetylcholine receptor (AChR) epsilon subunit gene in patients with sporadic or autosomal recessive congenital myasthenic syndromes (CMS).

PMID
10534268

Publication types

Research Support, Non-U.S. Gov't