Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene.

Shimozawa, Nobuyuki

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

Publication Type: Journal Article

0065-2598

10.1007/978-1-4419-9072-3_10 doi


Chondrodysplasia Punctata, Rhizomelic--genetics
Founder Effect
Haplotypes
Humans
Infant, Newborn
Japan
Mutation
Peroxins
Peroxisomal Disorders--genetics
Receptors, Cytoplasmic and Nuclear--genetics
Zellweger Syndrome--genetics