Jedrzejowska, H <br/><br/>
Uncompacted myelin in hereditary neuropathy with liability to pressure palsies with the 17 p11.2 deletion.  [electronic resource] 

 -  Folia neuropathologica  1999 
 - 220-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1641-4640 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 17--genetics<br/>Female<br/>Genetic Predisposition to Disease<br/>Humans<br/>Male<br/>Myelin Sheath--pathology<br/>Paralysis--genetics<br/>Pedigree<br/>Peripheral Nervous System Diseases--genetics<br/>Sural Nerve--injuries