Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Four frequently observed polymorphisms in the 3'-UTR of human peripheral myelin protein 22 (PMP22): identification of different haplotypes.

Clinical genetics - 1 Jun 1996

Young P, Wiebusch H, Stögbauer F, Ringelstein B, Assmann G, Funke H

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 17
Share to PMP22 gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Markers

Share to Haplotypes

Share to Myelin Proteins

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 8884085
DOI: 10.1111/j.1399-0004.1996.tb03799.x

Genes

PMP22

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Four frequently observed polymorphisms in the 3'-UTR of human peripheral myelin protein 22 (PMP22): identification of different haplotypes.PMID 8884085Read ↗

Exonic SNPs at positions 220 (A/G) and 445 (C/T) of the peripheral myelin protein 2 (PMP2).Semantic proximity Read ↗

The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplicationSemantic proximity Read ↗

The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1ASemantic proximity Read ↗

A novel stop codon mutation in the PMP22 gene associated with a variable phenotype.Semantic proximity Read ↗

Polymorphisms involving the transmembrane domains of human TAP2.Semantic proximity Read ↗

A new polymorphism in the flanking region of human VAMP2 and hPer1 genes.Semantic proximity Read ↗

A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence.Semantic proximity Read ↗

Mutations of the same sequence of the myelin P0 gene causing two different phenotypes.Semantic proximity Read ↗

Frequency of mutations in the early growth response 2 gene associated with peripheral demyelinating neuropathies.Semantic proximity Read ↗

Single nucleotide polymorphism in a commonly utilized LAMB3 primer sequence: implications for mutation detection and haplotype analysis in junctional epidermolysis bullosa.Semantic proximity Read ↗

Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies.Semantic proximity Read ↗

Peripheral myelin protein-22 gene deletion in two unrelated Japanese pedigrees with hereditary neuropathy with liability to pressure palsies.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.