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

Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Gaza Strip Palestinians.

Blood cells, molecules & diseases - 1 Jan 2000

Sirdah Mahmoud, Reading N Scott, Vankayalapati Hariprasad, Perkins Sherrie L, Shubair Mohammad E, Aboud Lina, Roper David, Prchal Josef T

Abstract excerpt

BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency, affecting more than 500 million people worldwide, is one of the most common of inherited disorders. There are 186 G6PD mutations published, with mutational clustering within defined ethnic/racial groups. However comprehensive molecu...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Arabs
Share to Child, Preschool
Share to Exons

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glucosephosphate Dehydrogenase

Share to Glucosephosphate Dehydrogenase Deficiency

Share to Hemolysis

Share to Introns

Share to Middle East

Source

Identifiers

PMID: 22770933
DOI: 10.1016/j.bcmd.2012.06.003

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22770933-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Gaza Strip Palestinians.PMID 22770933Read ↗

Hemolysis and Mediterranean G6PD mutation (c.563 C>T) and c.1311 C>T polymorphism among Palestinians at Gaza Strip.Semantic proximity Read ↗

Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same community.Semantic proximity Read ↗

The ethnogeographic variability of genetic factors underlying G6PD deficiency.Semantic proximity Read ↗

Molecular characterization of glucose-6-phosphate dehydrogenase deficiency among Jordanians.Semantic proximity Read ↗

Possible association of 3' UTR +357 A>G, IVS11-nt 93 T>C, c.1311 C>T polymorphism with G6PD deficiency.Semantic proximity Read ↗

Glucose-6-phosphate dehydrogenase deficiencySemantic proximity Read ↗

Frequency of Mediterranean mutation among a group of Saudi G6PD patients in Western region-Jeddah.Semantic proximity Read ↗

Molecular characterization of glucose-6-phosphate dehydrogenase gene defect in the Kuwaiti population.Semantic proximity Read ↗

Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Al-Ain District, United Arab Emirates.Semantic proximity Read ↗

Genetic, Clinical, and Biochemical Characterization of a Large Cohort of Palestinian Patients With Fanconi-Bickel Syndrome.Semantic proximity Read ↗

MEFV genotype distribution and allele frequencies in familial Mediterranean fever: a 20-year retrospective study of 2,246 individuals from a Palestinian laboratory archiveSemantic proximity Read ↗

Molecular Heterogeneity of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in the Portuguese Population.Semantic proximity Read ↗

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