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

A spontaneous mutation produced a novel elongated beta-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotype.

Blood - 15 Mar 1990

Ristaldi M S, Pirastu M, Murru S, Casula L, Loudianos G, Cao A, Sciarratta G V, Agosti S, Parodi M I, Leone D

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 Amino Acid Sequence
Share to Base Sequence
Share to Genetic Variation
Share to Globins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hemoglobins, Abnormal

Share to Molecular Sequence Data

Share to Phenotype

Share to Thalassemia

Source

Identifiers

PMID: 2310835

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A spontaneous mutation produced a novel elongated beta-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotype.PMID 2310835Read ↗

Novel and unusual deletion-insertion thalassemic mutation in exon 1 of the beta-globin gene.Semantic proximity Read ↗

Novel, de novo, beta-globin variant with decreased oxygen affinity (HBB:c.317T>A, "Hemoglobin St. George") in a healthy child with low oxygen saturations and anemia.Semantic proximity Read ↗

A rare complex rearrangement in the β-globin gene cluster causing a novel homozygous G γ(A γδβ)0 -thalassemia.Semantic proximity Read ↗

Hb Antalya [codons 3-5 (Leu-Thr-Pro-->Ser-Asp-Ser)]: a new unstable variant leading to chronic microcytic anemia and high Hb A2.Semantic proximity Read ↗

Two new Ggamma chain variants: Hb F-clamart [gamma17(A14)Lys-->Asn] and Hb F-Ouled Rabah [gamma19(B1)Asn-->Lys].Semantic proximity Read ↗

Hb aubagne [beta64(E8)Gly-Ala]: a new unstable beta chain variant found in a French family.Semantic proximity Read ↗

Hb Limassol [beta8(A5)Lys-->Asn]: a new hemoglobin variant.Semantic proximity Read ↗

Hb Jambol: a new hyperunstable hemoglobin causing severe hemolytic anemia.Semantic proximity Read ↗

Eight-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta khon kaen) with an inclusion body beta-thalassemia trait.Semantic proximity Read ↗

Structural alterations of the gamma-globin genes in a Brazilian population.Semantic proximity Read ↗

Hb Evora [alpha 2-35, Ser-->Pro], a novel hemoglobin variant associated with an alpha-thalassemia phenotype.Semantic proximity Read ↗

Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy.Semantic proximity Read ↗

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