Zafeiriou, D I <br/><br/>
Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy.  [electronic resource] 

 -  Pediatric research  Mar 2001 
 - 407-12 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0031-3998 
<br/><br/><label>Standard No.: </label>10.1203/00006450-200103000-00016  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Cockayne Syndrome--genetics<br/>DNA-Binding Proteins--genetics<br/>Endonucleases<br/>Female<br/>Humans<br/>Infant<br/>Mutation<br/>Nuclear Proteins<br/>Transcription Factors<br/>Xeroderma Pigmentosum--genetics