Shimozawa, Nobuyuki <br/><br/>
Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene.  [electronic resource] 

 -  Advances in experimental medicine and biology  2003 
 - 71 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0065-2598 
<br/><br/><label>Standard No.: </label>10.1007/978-1-4419-9072-3_10  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chondrodysplasia Punctata, Rhizomelic--genetics<br/>Founder Effect<br/>Haplotypes<br/>Humans<br/>Infant, Newborn<br/>Japan<br/>Mutation<br/>Peroxins<br/>Peroxisomal Disorders--genetics<br/>Receptors, Cytoplasmic and Nuclear--genetics<br/>Zellweger Syndrome--genetics