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Article

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

Advances in experimental medicine and biology - 1 Jan 2003

Shimozawa Nobuyuki, Nagase Tomoko, Takemoto Yasuhiko, Suzuki Yasuyuki, Kondo Naomi

Abstract excerpt

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Share to Founder Effect
Share to Haplotypes
Share to Infant, Newborn
Share to Japan

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Peroxins

Share to Peroxisomal Disorders

Share to Receptors, Cytoplasmic and Nuclear

Share to Zellweger Syndrome

Source

Identifiers

PMID: 14713216
DOI: 10.1007/978-1-4419-9072-3_10

Genes

PEX10

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene.PMID 14713216Read ↗

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