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

Duchenne gene carrier as cause of asymptomatic hyperckemia.

Arquivos de neuro-psiquiatria - 1 Jun 2008

Almeida Diogo Fraxino de, Melo Aluisio Cláudio Mentor Couto, Bittencourt Paulo Rogério M de

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 Biopsy
Share to Blotting, Southern
Share to Creatine Kinase
Share to Dystrophin

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Carrier Screening

Share to Metabolic Diseases

Share to Muscle, Skeletal

Share to Muscular Dystrophy, Duchenne

Source

Identifiers

PMID: 18641889
DOI: 10.1590/s0004-282x2008000300032

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

Duchenne gene carrier as cause of asymptomatic hyperckemia.PMID 18641889Read ↗

Atypical haemolytic uraemic syndrome in a Japanese patient with DGKE genetic mutations.Semantic proximity Read ↗

A novel mutation of congenital factor V deficiency in Henoch-Schönlein purpura.Semantic proximity Read ↗

Genetic mutations causing hereditary cholestasis.Semantic proximity Read ↗

Closing in on a "familial cholestasis gene".Semantic proximity Read ↗

Unsuspected mutation in a family with congenital adrenal hyperplasia.Semantic proximity Read ↗

A Caucasian population with a high frequency of Au 'carriers': genetic analysis of the condition.Semantic proximity Read ↗

Complete DiGeorge syndrome associated with CHD7 mutation.Semantic proximity Read ↗

STAR gene mutation in a patient with congenital lipoid adrenal hyperplasia.Semantic proximity Read ↗

Mutations of human butyrylcholinesterase gene in a family with hypocholinesterasemia.Semantic proximity Read ↗

Congenital Glucose-Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene.Semantic proximity Read ↗

Novel mutation causing Hermansky-Pudlak Syndrome Type 2.Semantic proximity Read ↗

Familial ACD with no recognizable enzyme abnormalities.Semantic proximity Read ↗

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