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

EDA mutation by exome sequencing in non-syndromic X-linked oligodontia.

Clinical genetics - 1 Aug 2017

Martins L, Machado R A, Araujo D S, Giovani P A, Rebouças P D, Rodrigues L P, Mofatto L S, Ribeiro M M, Coutinho L L, Puppin-Rontani R M, Coletta R D, Nociti F H, Kantovitz K R

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 Anodontia
Share to Brazil
Share to Computer Simulation
Share to Ectodysplasins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Exome Sequencing

Share to Genetic Diseases, X-Linked

Share to Models, Molecular

Share to Protein Conformation

Source

Identifiers

PMID: 28052341
DOI: 10.1111/cge.12961

Genes

EDA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

EDA mutation by exome sequencing in non-syndromic X-linked oligodontia.PMID 28052341Read ↗

EDA mutation as a cause of hypohidrotic ectodermal dysplasia: a case report and review of the literature.Semantic proximity Read ↗

Oligodontia and curly hair occur with ectodysplasin-a mutations.Semantic proximity Read ↗

Identified a novel splicing mutation at EDA gene in a hypohidrotic ectodermal dysplasia pedigree.Semantic proximity Read ↗

Mutation Screening of the EDA Gene in Seven Chinese Families with X-Linked Hypohidrotic Ectodermal Dysplasia.Semantic proximity Read ↗

Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands.Semantic proximity Read ↗

Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR- and EDA-associated nonsyndromic oligodontia.Semantic proximity Read ↗

Novel insight into the ectodermal dysplasia 11A: Splicing variant of the EDARADD gene in a family with clinical variability and literature review.Semantic proximity Read ↗

[Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia].Semantic proximity Read ↗

Novel EDA mutations cause X-linked hypohidrotic ectodermal dysplasia: the first study from Venezuela.Semantic proximity Read ↗

Novel missense mutation in the EDA gene in a family affected by oligodontia.Semantic proximity Read ↗

Analyses of oligodontia phenotypes and genetic etiologies.Semantic proximity Read ↗

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