Neumann, S <br/><br/>
Identification of new mutations in Israeli patients with X-linked adrenoleukodystrophy.  [electronic resource] 

 -  Genetic testing  2001 
 - 65-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1090-6576 
<br/><br/><label>Standard No.: </label>10.1089/109065701750168806  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenoleukodystrophy--genetics<br/>Arabs--genetics<br/>Base Sequence<br/>Codon, Nonsense--genetics<br/>DNA Mutational Analysis<br/>Exons<br/>Female<br/>Founder Effect<br/>Frameshift Mutation--genetics<br/>Genetic Linkage--genetics<br/>Heterozygote<br/>Humans<br/>Israel<br/>Jews--genetics<br/>Male<br/>Morocco--ethnology<br/>Mutation--genetics<br/>Mutation, Missense--genetics<br/>Pedigree<br/>X Chromosome--genetics