Korinthenberg, R <br/><br/>
Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region.  [electronic resource] 

 -  Annals of neurology  Sep 1997 
 - 364-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>0364-5134 
<br/><br/><label>Standard No.: </label>10.1002/ana.410420314  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Axons--pathology<br/>Brain Stem--pathology<br/>Chromosomes, Human, Pair 5<br/>Female<br/>Gene Deletion<br/>Hereditary Sensory and Autonomic Neuropathies--complications<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Microscopy, Electron<br/>Muscle, Skeletal--ultrastructure<br/>Neurons, Afferent--pathology<br/>Phenotype<br/>Spinal Muscular Atrophies of Childhood--complications<br/>Sural Nerve--ultrastructure