Ohno, K <br/><br/>
Frameshifting and splice-site mutations in the acetylcholine receptor epsilon subunit gene in three Turkish kinships with congenital myasthenic syndromes.  [electronic resource] 

 -  Annals of the New York Academy of Sciences  May 1998 
 - 189-94 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0077-8923 
<br/><br/><label>Standard No.: </label>10.1111/j.1749-6632.1998.tb10926.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Alternative Splicing<br/>Child<br/>Female<br/>Frameshift Mutation<br/>Humans<br/>Macromolecular Substances<br/>Male<br/>Models, Molecular<br/>Myasthenia Gravis--congenital<br/>Nuclear Family<br/>Pedigree<br/>Protein Conformation<br/>Receptors, Cholinergic--deficiency<br/>Syndrome<br/>Turkey