Williams, R <br/><br/>
Genetic heterogeneity in neuronal ceroid lipofuscinosis (NCL): evidence that the late-infantile subtype (Jansky-Bielschowsky disease; CLN2) is not an allelic form of the juvenile or infantile subtypes.  [electronic resource] 

 -  American journal of human genetics  Oct 1993 
 - 931-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Child, Preschool<br/>Chromosomes, Human, Pair 1<br/>Chromosomes, Human, Pair 16<br/>Female<br/>Genetic Linkage<br/>Humans<br/>Infant<br/>Male<br/>Neuronal Ceroid-Lipofuscinoses--classification<br/>Tripeptidyl-Peptidase 1