Boylan, K B <br/><br/>
Autosomal dominant distal spinal muscular atrophy in four generations.  [electronic resource] 

 -  Neurology  Apr 1995 
 - 699-704 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>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.45.4.699  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Charcot-Marie-Tooth Disease--genetics<br/>Female<br/>Genetic Linkage<br/>Humans<br/>Male<br/>Middle Aged<br/>Muscles--pathology<br/>Muscular Atrophy, Spinal--genetics<br/>Nervous System--pathology<br/>Nervous System Physiological Phenomena<br/>Neural Conduction--physiology<br/>Pedigree