TY  - GEN
AU  - Shimozawa,Nobuyuki
AU  - Nagase,Tomoko
AU  - Takemoto,Yasuhiko
AU  - Suzuki,Yasuyuki
AU  - Kondo,Naomi
TI  - Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene
SN  - 0065-2598
PY  - 2004///0702
KW  - Chondrodysplasia Punctata, Rhizomelic
KW  - genetics
KW  - Founder Effect
KW  - Haplotypes
KW  - Humans
KW  - Infant, Newborn
KW  - Japan
KW  - Mutation
KW  - Peroxins
KW  - Peroxisomal Disorders
KW  - Receptors, Cytoplasmic and Nuclear
KW  - Zellweger Syndrome
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1007/978-1-4419-9072-3_10
ER  -