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

[More mutations responsible for copper overload].

Tijdschrift voor diergeneeskunde - 1 Mar 2011

Haneveld Johan Klein

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 Species Specificity
Share to Biomarkers
Share to Copper
Share to Dog Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to Risk Factors

Source

Identifiers

PMID: 21442845

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[More mutations responsible for copper overload].PMID 21442845Read ↗

[Genetics of iron overload].Semantic proximity Read ↗

[From gene to disease: copper-transporting P ATPases alteration].Semantic proximity Read ↗

[Contribution of molecular genetics in understanding iron metabolism].Semantic proximity Read ↗

[Copper metabolism and genetic disorders].Semantic proximity Read ↗

[Processing enzymes: more fat mutations].Semantic proximity Read ↗

Inherited disorders of transition metal metabolism: an update.Semantic proximity Read ↗

[Practical use of genetic markers other than C282Y in iron overload disorders].Semantic proximity Read ↗

Genetic iron overload disordersSemantic proximity Read ↗

Unresolved questions in human copper pump mechanisms.Semantic proximity Read ↗

Copper transport and its alterations in Menkes and Wilson diseases.Semantic proximity Read ↗

[Hereditary hypouricemia].Semantic proximity Read ↗

The molecular basis of copper-transport diseases.Semantic proximity Read ↗

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