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Article

Heterozygous somatic activating AKT1 mutation in a case of Proteus syndrome with mental retardation.

The Journal of dermatology - 1 Feb 2014

Yang Zhou, Xu Zhe, Sun Yu-Juan, Ma Lin

Abstract excerpt

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Share to Child, Preschool
Share to AKT1 gene
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Proto-Oncogene Proteins c-akt

Source

Identifiers

PMID: 24387135
DOI: 10.1111/1346-8138.12358

Genes

AKT1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Heterozygous somatic activating AKT1 mutation in a case of Proteus syndrome with mental retardation.PMID 24387135Read ↗

A Mosaic Activating Mutation in AKT1 Associated with the Proteus SyndromeSemantic proximity Read ↗

A mosaic activating mutation in AKT1 associated with the Proteus syndrome.Semantic proximity Read ↗

Extending the spectrum of AKT1 mosaicism: not just the Proteus syndrome.Semantic proximity Read ↗

High-level somatic mosaicism of AKT1 c.49G>A mutation in skin scrapings from epidermal nevi enables non-invasive molecular diagnosis in patients with Proteus syndrome.Semantic proximity Read ↗

A limited form of proteus syndrome with bilateral plantar cerebriform collagenomas and varicose veins secondary to a mosaic AKT1 mutation.Semantic proximity Read ↗

Phenotype and genotype of AKT3-related disorders.Semantic proximity Read ↗

Turkish cases of Mabry Syndrome with a novel homozygous mutation in PGAP2 geneSemantic proximity Read ↗

Prenatal diagnosis of Proteus syndrome: Diagnosis of an AKT1 mutation from amniocytes.Semantic proximity Read ↗

Mirror syndromes regarding AKT3 mutations: Loss of function variant leading to microcephaly.Semantic proximity Read ↗

Identification of a Mosaic Activating Mutation in GNA11 in Atypical Sturge-Weber SyndromeSemantic proximity Read ↗

An activating mutation in AKT1 in human prostate cancer.Semantic proximity Read ↗

Somatic mutation of PIK3R1 gene is rare in common human cancers.Semantic proximity Read ↗

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