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

Clinical utility gene card for: HMSN/HNPP HMSN types 1, 2, 3, 6 (CMT1,2,4, DSN, CHN, GAN, CCFDN, HNA); HNPP.

European journal of human genetics : EJHG - 1 Sept 2010

Aretz Stefan, Rautenstrauss Bernd, Timmerman Vincent

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 Hereditary Sensory and Motor Neuropathy
Share to Mutation

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 20512157
DOI: 10.1038/ejhg.2010.75
PMCID: PMC2987431

Genes

GAN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical utility gene card for: HMSN/HNPP HMSN types 1, 2, 3, 6 (CMT1,2,4, DSN, CHN, GAN, CCFDN, HNA); HNPP.PMID 20512157Read ↗

Clinical utility gene card for: Zellweger syndrome spectrum.Semantic proximity Read ↗

Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches.Semantic proximity Read ↗

Clinical utility gene card for: von Hippel-Lindau (VHL).Semantic proximity Read ↗

Clinical utility gene card for: 3-M syndrome - update 2013.Semantic proximity Read ↗

Clinical utility gene card for: Lesch-Nyhan syndrome--update 2013.Semantic proximity Read ↗

Clinical utility gene card for: Multi-minicore disease.Semantic proximity Read ↗

Clinical utility gene card for: Central core disease.Semantic proximity Read ↗

Clinical utility gene card for: CHARGE syndrome - update 2015.Semantic proximity Read ↗

Clinical utility gene card for: Alström syndrome.Semantic proximity Read ↗

Clinical utility gene card for: Ehlers-Danlos syndrome types I-VII and variants - update 2012.Semantic proximity Read ↗

Gene table of monogenic neuromuscular disorders (nuclear genome only) Vol. 18 No. 1, January 2008.Semantic proximity Read ↗

Clinical utility gene card for: Nemaline myopathy - update 2015.Semantic proximity Read ↗

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