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

Congenital analbuminemia attributable to compound heterozygosity for novel mutations in the albumin gene.

Clinical chemistry - 1 Jul 2005

Campagna Filomena, Fioretti Francesca, Burattin Marco, Romeo Stefano, Sentinelli Federica, Bifolco Maura, Sirinian Maria Isabella, Del Ben Maria, Angelico Francesco, Arca Marcello

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 Heterozygote
Share to Mutation
Share to Polymorphism, Restriction Fragment Length

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Single-Stranded Conformational

Share to Serum Albumin

Source

Identifiers

PMID: 15976105
DOI: 10.1373/clinchem.2005.048561

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

Congenital analbuminemia attributable to compound heterozygosity for novel mutations in the albumin gene.PMID 15976105Read ↗

Congenital Analbuminemia in Unrelated Algerian and Turkish Families is Caused by the Same Molecular Defect in the Albumin Gene.Semantic proximity Read ↗

A novel nonsense variation in the albumin gene (c.1309 A>T) causing analbuminaemia.Semantic proximity Read ↗

Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene.Semantic proximity Read ↗

Analbuminemia: three cases resulting from different point mutations in the albumin gene.Semantic proximity Read ↗

A novel insertion (c.1098dupT) in the albumin gene causes analbuminemia in a consanguineous family.Semantic proximity Read ↗

Congenital analbuminaemia: molecular defects and biochemical and clinical aspects.Semantic proximity Read ↗

Analbuminemia produced by a novel splicing mutation.Semantic proximity Read ↗

[Congenital analbuminemia].Semantic proximity Read ↗

A novel splicing mutation in the ALB gene causing analbuminaemia in a Portuguese woman.Semantic proximity Read ↗

Albumin locust valley: a new case of analbuminemia.Semantic proximity Read ↗

A novel splicing mutation causes an undescribed type of analbuminemia.Semantic proximity Read ↗

A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia.Semantic proximity Read ↗

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