Discover Community Create You

t/gene-gjb1

GJB1 gene

Discuss publications and research concerning the GJB1 gene.

0 followers0 posts13 articles

Create Post

TitleDiscussionLink a PMID (optional)

All posts discussion question review note

Create the first post

Ask a question, share an idea or link scientific evidence.

Topic rules

Follow Noodle’s community and scientific integrity rules.

Moderators

Managed by the Noodle moderation team.

Related literature

Diseases of connexins expressed in myelinating glia.
GJB1
A case with CMTX1 disease showing transient ischemic-attack-like episodes.
GJB1
Connexins, gap junctions and peripheral neuropathy.
GJB1
Emery-Dreifuss muscular dystrophy type 2 associated (?) with mild peripheral polyneuropathy.
GJB1
Intermediate Charcot-Marie-Tooth disease.
GJB1
X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutation.
GJB1
Segregation analysis in families with Charcot-Marie-Tooth disease allows reclassification of putative disease causing mutations.
GJB1
Novel GJB1 mutation causing adult-onset Charcot-Marie-Tooth disease in a female patient.
GJB1
Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing.
GJB1
[Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease].
GJB1

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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