Evidence map›Paper›PMID 41037005›Full record

ArticleTurkish journal of haematology : official journal of Turkish Society of Haematology2025

Spectrum of Factor VIII Gene Variants in 78 Patients with Hemophilia A in Guangxi Province, China, Including Nine Novel Variants: A Descriptive Study

Jiali Jiang, Jinxia Jiang, Yuping Li, Lifang Huang, Hongying Wei

Abstract read
In one paragraph

Article in Turkish journal of haematology : official journal of Turkish Society of Haematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Jiali JiangThe Second Affiliated Hospital of Guangxi Medical University, Department of Pediatrics, Nanning, P.R. ChinaORCID 0000-0001-5757-5575
Jinxia JiangMaternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Department of Pediatric Hematology and Oncology, Nanning, Guangxi, P.R. ChinaORCID 0009-0005-4040-5322
Yuping LiThe Second Affiliated Hospital of Guangxi Medical University, Department of Pediatrics, Nanning, P.R. ChinaORCID 0009-0002-8886-8893
Lifang HuangMaternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Department of Pediatric Hematology and Oncology, Nanning, Guangxi, P.R. ChinaORCID 0000-0002-6339-2115
Hongying WeiThe Second Affiliated Hospital of Guangxi Medical University, Department of Pediatrics, Nanning, P.R. ChinaORCID 0009-0008-1694-6024

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Hemophilia A (HA) is an X-linked hereditary bleeding disorder caused by variants in the coagulation factor VIII ( Materials and Methods: Long-distance PCR was used to detect intron inversions and next-generation sequencing gene panels were used to identify small sequence variants. Results: Fifty-two different Conclusion: The

Indexed as

Factor VIIIGenetic VariationHemophilia AMutationAdolescentAdultChildChild, PreschoolChinaFemaleGenetic Association StudiesHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedF8 protein, humanFactor VIIIF8Factor VIIIHemophilia Anext-generation sequencingvariant spectrum

Identifiers

PMID41037005
PMCPMC12671265

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.